Canonical Allele Identifier: CA975105335
Gene: ABCC6 HGNC NCBI

Linked Data

dbSNP Id: rs2046489744

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16154818A>G , CM000678.2:g.16154818A>G GRCh38
NC_000016.9:g.16248675A>G , CM000678.1:g.16248675A>G GRCh37
NC_000016.8:g.16156176A>G NCBI36
NG_007558.2:g.73654T>C
NG_007558.3:g.73800T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000576204.6:n.905-24T>C
ENST00000622290.5:c.*214-24T>C ENSP00000483331.2:n.*214-24T>C
ENST00000205557.12:c.4042-24T>C MANE Select ENSP00000205557.7:n.4042-24T>C
ENST00000640696.1:c.856-24T>C ENSP00000492197.1:n.856-24T>C
ENST00000205557.11:c.4042-24T>C ENSP00000205557.7:n.4042-24T>C
ENST00000456970.6:c.3667-24T>C ENSP00000405002.2:n.3667-24T>C
ENST00000576204.5:n.905-24T>C
ENST00000622290.4:c.*1251-24T>C ENSP00000483331.1:n.*1251-24T>C
NM_001171.5:c.4042-24T>C NP_001162.4:n.4042-24T>C
XM_011522479.1:c.4009-24T>C XP_011520781.1:n.4009-24T>C
XM_011522480.1:c.3700-24T>C XP_011520782.1:n.3700-24T>C
XM_011522481.1:c.3700-24T>C XP_011520783.1:n.3700-24T>C
XR_933134.1:n.539-4963A>G
NM_001351800.1:c.3700-24T>C NP_001338729.1:n.3700-24T>C
NR_147784.1:n.3704-24T>C
XM_011522479.2:c.4009-24T>C XP_011520781.1:n.4009-24T>C
XM_011522481.3:c.3700-24T>C XP_011520783.1:n.3700-24T>C
XM_017023212.1:c.3874-24T>C XP_016878701.1:n.3874-24T>C
XM_024450261.1:c.4078-24T>C XP_024306029.1:n.4078-24T>C
NM_001171.6:c.4042-24T>C MANE Select NP_001162.5:n.4042-24T>C