Canonical Allele Identifier: CA394883019

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16259583A>G (hg19) ; chr16:g.16165726A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16165726A>G , CM000678.2:g.16165726A>G	GRCh38
NC_000016.9:g.16259583A>G , CM000678.1:g.16259583A>G	GRCh37
NC_000016.8:g.16167084A>G	NCBI36
NG_007558.2:g.62746T>C
NG_007558.3:g.62892T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3203T>C	ENSP00000483331.2:p.Met1068Thr
ENST00000205557.12:c.3203T>C MANE Select	ENSP00000205557.7:p.Met1068Thr
ENST00000640696.1:c.218T>C	ENSP00000492197.1:p.Met73Thr
ENST00000205557.11:c.3203T>C	ENSP00000205557.7:p.Met1068Thr
ENST00000456970.6:c.3028T>C	ENSP00000405002.2:n.3028T>C
ENST00000622290.4:c.*412T>C	ENSP00000483331.1:n.*412T>C
NM_001171.5:c.3203T>C	NP_001162.4:p.Met1068Thr
XM_011522479.1:c.3170T>C	XP_011520781.1:p.Met1057Thr
XM_011522480.1:c.2861T>C	XP_011520782.1:p.Met954Thr
XM_011522481.1:c.2861T>C	XP_011520783.1:p.Met954Thr
XR_932836.1:n.3438T>C
XR_932837.1:n.3439T>C
XR_932838.1:n.3439T>C
NM_001351800.1:c.2861T>C	NP_001338729.1:p.Met954Thr
NR_147784.1:n.3065T>C
XM_011522479.2:c.3170T>C	XP_011520781.1:p.Met1057Thr
XM_011522481.3:c.2861T>C	XP_011520783.1:p.Met954Thr
XM_017023212.1:c.3035T>C	XP_016878701.1:p.Met1012Thr
XM_017023214.1:c.3203T>C	XP_016878703.1:p.Met1068Thr
XM_024450261.1:c.3239T>C	XP_024306029.1:p.Met1080Thr
XR_932836.2:n.3384T>C
XR_932837.3:n.3384T>C
XR_932838.3:n.3384T>C
NM_001171.6:c.3203T>C MANE Select	NP_001162.5:p.Met1068Thr