Canonical Allele Identifier: CA489740044

Gene: IVD

Linked Data

• ClinVar Variation Id: 2746683
• ClinVar RCV Id: RCV003501940
• dbSNP Id: rs1430512539
• MyVariant Identifiers: chr15:g.40703497T>C (hg19) ; chr15:g.40411298T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40411298T>C , CM000677.2:g.40411298T>C	GRCh38
NC_000015.9:g.40703497T>C , CM000677.1:g.40703497T>C	GRCh37
NC_000015.8:g.38490789T>C	NCBI36
NG_011986.1:g.10812T>C
NG_011986.2:g.10814T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.405T>C	ENSP00000417990.3:p.Ser135=
ENST00000487418.8:c.495T>C MANE Select	ENSP00000418397.3:p.Ser165=
ENST00000610693.5:c.582T>C	ENSP00000479359.2:p.Ser194=
ENST00000650656.1:c.414T>C	ENSP00000498731.1:p.Ser138=
ENST00000651168.1:c.504T>C	ENSP00000499074.1:p.Ser168=
ENST00000473112.6:c.254T>C
ENST00000479013.6:c.414T>C	ENSP00000417990.2:p.Ser138=
ENST00000481262.6:c.101T>C
ENST00000484250.1:n.118T>C
ENST00000487418.6:c.504T>C	ENSP00000418397.2:p.Ser168=
ENST00000558610.5:c.447T>C	ENSP00000453821.1:p.Ser149=
ENST00000610693.4:c.591T>C	ENSP00000479359.1:p.Ser197=
NM_001159508.1:c.414T>C	NP_001152980.1:p.Ser138=
NM_002225.3:c.504T>C	NP_002216.2:p.Ser168=
XM_005254350.2:c.504T>C	XP_005254407.1:p.Ser168=
XM_005254356.2:c.504T>C	XP_005254413.1:p.Ser168=
XM_006720491.2:c.447T>C	XP_006720554.1:p.Ser149=
XM_006720492.2:c.504T>C	XP_006720555.1:p.Ser168=
XM_006720493.2:c.504T>C	XP_006720556.1:p.Ser168=
XM_006720494.2:c.504T>C	XP_006720557.1:p.Ser168=
XM_006720495.2:c.504T>C	XP_006720558.1:p.Ser168=
XM_011521523.1:c.504T>C	XP_011519825.1:p.Ser168=
XM_011521524.1:c.504T>C	XP_011519826.1:p.Ser168=
XR_243097.3:n.504T>C
XR_243098.2:n.504T>C
XR_429453.2:n.605T>C
NM_001159508.2:c.405T>C	NP_001152980.2:p.Ser135=
NM_001354597.2:c.447T>C	NP_001341526.1:p.Ser149=
NM_001354598.2:c.495T>C	NP_001341527.2:p.Ser165=
NM_001354599.2:c.582T>C	NP_001341528.2:p.Ser194=
NM_001354600.2:c.582T>C	NP_001341529.2:p.Ser194=
NM_001354601.2:c.495T>C	NP_001341530.2:p.Ser165=
NM_002225.4:c.495T>C	NP_002216.3:p.Ser165=
NR_148925.1:n.905T>C
XM_006720495.3:c.504T>C	XP_006720558.1:p.Ser168=
XM_017022149.1:c.591T>C	XP_016877638.1:p.Ser197=
XM_017022150.1:c.591T>C	XP_016877639.1:p.Ser197=
XM_017022153.1:c.591T>C	XP_016877642.1:p.Ser197=
XM_017022154.2:c.534T>C	XP_016877643.1:p.Ser178=
XM_017022155.2:c.591T>C	XP_016877644.1:p.Ser197=
XM_017022157.1:c.591T>C	XP_016877646.1:p.Ser197=
XM_017022158.2:c.591T>C	XP_016877647.1:p.Ser197=
XR_001751263.1:n.854T>C
XR_001751264.1:n.895T>C
NM_001159508.3:c.405T>C	NP_001152980.2:p.Ser135=
NM_001354597.3:c.447T>C	NP_001341526.1:p.Ser149=
NM_001354598.3:c.495T>C	NP_001341527.2:p.Ser165=
NM_001354599.3:c.582T>C	NP_001341528.2:p.Ser194=
NM_001354600.3:c.582T>C	NP_001341529.2:p.Ser194=
NM_001354601.3:c.495T>C	NP_001341530.2:p.Ser165=
NM_002225.5:c.495T>C MANE Select	NP_002216.3:p.Ser165=
NR_148925.2:n.907T>C