Canonical Allele Identifier: CA493798073

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16253429T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159572T>G , CM000678.2:g.16159572T>G	GRCh38
NC_000016.9:g.16253429T>G , CM000678.1:g.16253429T>G	GRCh37
NC_000016.8:g.16160930T>G	NCBI36
NG_007558.2:g.68900A>C
NG_007558.3:g.69046A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3645A>C	ENSP00000483331.2:p.Thr1215=
ENST00000205557.12:c.3645A>C MANE Select	ENSP00000205557.7:p.Thr1215=
ENST00000640696.1:c.459A>C	ENSP00000492197.1:p.Thr153=
ENST00000205557.11:c.3645A>C	ENSP00000205557.7:p.Thr1215=
ENST00000456970.6:c.3270A>C	ENSP00000405002.2:n.3270A>C
ENST00000622290.4:c.*854A>C	ENSP00000483331.1:n.*854A>C
NM_001171.5:c.3645A>C	NP_001162.4:p.Thr1215=
XM_011522479.1:c.3612A>C	XP_011520781.1:p.Thr1204=
XM_011522480.1:c.3303A>C	XP_011520782.1:p.Thr1101=
XM_011522481.1:c.3303A>C	XP_011520783.1:p.Thr1101=
XR_932836.1:n.3880A>C
XR_932837.1:n.3681A>C
XR_932838.1:n.3681A>C
XR_933134.1:n.539-209T>G
NM_001351800.1:c.3303A>C	NP_001338729.1:p.Thr1101=
NR_147784.1:n.3307A>C
XM_011522479.2:c.3612A>C	XP_011520781.1:p.Thr1204=
XM_011522481.3:c.3303A>C	XP_011520783.1:p.Thr1101=
XM_017023212.1:c.3477A>C	XP_016878701.1:p.Thr1159=
XM_024450261.1:c.3681A>C	XP_024306029.1:p.Thr1227=
XR_932836.2:n.3826A>C
XR_932837.3:n.3626A>C
XR_932838.3:n.3626A>C
NM_001171.6:c.3645A>C MANE Select	NP_001162.5:p.Thr1215=