Canonical Allele Identifier: CA195499123

Gene: SLC28A3

Linked Data

• dbSNP Id: rs972460069
• gnomAD v3: 9-84329448-A-G
• gnomAD v4: 9-84329448-A-G
• MyVariant Identifiers: chr9:g.86944363A>G (hg19) ; chr9:g.84329448A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84329448A>G , CM000671.2:g.84329448A>G	GRCh38
NC_000009.11:g.86944363A>G , CM000671.1:g.86944363A>G	GRCh37
NC_000009.10:g.86134183A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376238.5:c.60+11126T>C MANE Select	ENSP00000365413.4:n.60+11126T>C
ENST00000376238.4:c.60+11126T>C	ENSP00000365413.4:n.60+11126T>C
ENST00000495823.1:n.86+11126T>C
NM_001199633.1:c.60+11126T>C	NP_001186562.1:n.60+11126T>C
NM_022127.2:c.60+11126T>C	NP_071410.1:n.60+11126T>C
NR_037638.2:n.206+11126T>C
XM_011518905.1:c.60+11126T>C	XP_011517207.1:n.60+11126T>C
XM_011518906.1:c.60+11126T>C	XP_011517208.1:n.60+11126T>C
XM_011518907.1:c.-97-15994T>C	XP_011517209.1:n.-97-15994T>C
XM_011518909.1:c.60+11126T>C	XP_011517211.1:n.60+11126T>C
XM_011518910.1:c.60+11126T>C	XP_011517212.1:n.60+11126T>C
XR_929832.1:n.187+11126T>C
XM_011518905.2:c.60+11126T>C	XP_011517207.1:n.60+11126T>C
XM_011518906.2:c.60+11126T>C	XP_011517208.1:n.60+11126T>C
XM_011518907.2:c.-97-15994T>C	XP_011517209.1:n.-97-15994T>C
XM_011518909.2:c.60+11126T>C	XP_011517211.1:n.60+11126T>C
XM_011518910.2:c.60+11126T>C	XP_011517212.1:n.60+11126T>C
XR_929832.2:n.192+11126T>C
NM_001199633.2:c.60+11126T>C MANE Select	NP_001186562.1:n.60+11126T>C
NM_022127.3:c.60+11126T>C	NP_071410.1:n.60+11126T>C
NR_037638.3:n.185+11126T>C