Canonical Allele Identifier: CA394875564

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16248770C>G (hg19) ; chr16:g.16154913C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154913C>G , CM000678.2:g.16154913C>G	GRCh38
NC_000016.9:g.16248770C>G , CM000678.1:g.16248770C>G	GRCh37
NC_000016.8:g.16156271C>G	NCBI36
NG_007558.2:g.73559G>C
NG_007558.3:g.73705G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000576204.6:n.864G>C
ENST00000622290.5:c.*173G>C	ENSP00000483331.2:n.*173G>C
ENST00000205557.12:c.4001G>C MANE Select	ENSP00000205557.7:p.Gly1334Ala
ENST00000640696.1:c.815G>C	ENSP00000492197.1:p.Gly272Ala
ENST00000205557.11:c.4001G>C	ENSP00000205557.7:p.Gly1334Ala
ENST00000456970.6:c.3626G>C	ENSP00000405002.2:n.3626G>C
ENST00000576204.5:n.864G>C
ENST00000622290.4:c.*1210G>C	ENSP00000483331.1:n.*1210G>C
NM_001171.5:c.4001G>C	NP_001162.4:p.Gly1334Ala
XM_011522479.1:c.3968G>C	XP_011520781.1:p.Gly1323Ala
XM_011522480.1:c.3659G>C	XP_011520782.1:p.Gly1220Ala
XM_011522481.1:c.3659G>C	XP_011520783.1:p.Gly1220Ala
XR_933134.1:n.539-4868C>G
NM_001351800.1:c.3659G>C	NP_001338729.1:p.Gly1220Ala
NR_147784.1:n.3663G>C
XM_011522479.2:c.3968G>C	XP_011520781.1:p.Gly1323Ala
XM_011522481.3:c.3659G>C	XP_011520783.1:p.Gly1220Ala
XM_017023212.1:c.3833G>C	XP_016878701.1:p.Gly1278Ala
XM_024450261.1:c.4037G>C	XP_024306029.1:p.Gly1346Ala
NM_001171.6:c.4001G>C MANE Select	NP_001162.5:p.Gly1334Ala