Canonical Allele Identifier: CA394875402

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16248737A>C (hg19) ; chr16:g.16154880A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154880A>C , CM000678.2:g.16154880A>C	GRCh38
NC_000016.9:g.16248737A>C , CM000678.1:g.16248737A>C	GRCh37
NC_000016.8:g.16156238A>C	NCBI36
NG_007558.2:g.73592T>G
NG_007558.3:g.73738T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.897T>G
ENST00000622290.5:c.*206T>G	ENSP00000483331.2:n.*206T>G
ENST00000205557.12:c.4034T>G MANE Select	ENSP00000205557.7:p.Ile1345Ser
ENST00000640696.1:c.848T>G	ENSP00000492197.1:p.Ile283Ser
ENST00000205557.11:c.4034T>G	ENSP00000205557.7:p.Ile1345Ser
ENST00000456970.6:c.3659T>G	ENSP00000405002.2:n.3659T>G
ENST00000576204.5:n.897T>G
ENST00000622290.4:c.*1243T>G	ENSP00000483331.1:n.*1243T>G
NM_001171.5:c.4034T>G	NP_001162.4:p.Ile1345Ser
XM_011522479.1:c.4001T>G	XP_011520781.1:p.Ile1334Ser
XM_011522480.1:c.3692T>G	XP_011520782.1:p.Ile1231Ser
XM_011522481.1:c.3692T>G	XP_011520783.1:p.Ile1231Ser
XR_933134.1:n.539-4901A>C
NM_001351800.1:c.3692T>G	NP_001338729.1:p.Ile1231Ser
NR_147784.1:n.3696T>G
XM_011522479.2:c.4001T>G	XP_011520781.1:p.Ile1334Ser
XM_011522481.3:c.3692T>G	XP_011520783.1:p.Ile1231Ser
XM_017023212.1:c.3866T>G	XP_016878701.1:p.Ile1289Ser
XM_024450261.1:c.4070T>G	XP_024306029.1:p.Ile1357Ser
NM_001171.6:c.4034T>G MANE Select	NP_001162.5:p.Ile1345Ser