Canonical Allele Identifier: CA7925144
Gene: ABCC6 HGNC NCBI

Linked Data

ClinVar Variation Id: 433369
dbSNP Id: rs3902401

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16150116C>T , CM000678.2:g.16150116C>T GRCh38
NC_000016.9:g.16243973C>T , CM000678.1:g.16243973C>T GRCh37
NC_000016.8:g.16151474C>T NCBI36
NG_007558.2:g.78356G>A
NG_007558.3:g.78502G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000622290.5:c.*701G>A ENSP00000483331.2:n.*701G>A
ENST00000205557.12:c.*17G>A MANE Select ENSP00000205557.7:n.*17G>A
ENST00000640696.1:c.1343G>A ENSP00000492197.1:n.1343G>A
ENST00000205557.11:c.*17G>A ENSP00000205557.7:n.*17G>A
ENST00000576204.5:n.1392G>A
ENST00000622290.4:c.*1738G>A ENSP00000483331.1:n.*1738G>A
NM_001171.5:c.*17G>A NP_001162.4:n.*17G>A
XM_011522479.1:c.*17G>A XP_011520781.1:n.*17G>A
XM_011522480.1:c.*17G>A XP_011520782.1:n.*17G>A
XM_011522481.1:c.*17G>A XP_011520783.1:n.*17G>A
XR_933134.1:n.538+5826C>T
NM_001351800.1:c.*17G>A NP_001338729.1:n.*17G>A
NR_147784.1:n.4191G>A
XM_011522479.2:c.*17G>A XP_011520781.1:n.*17G>A
XM_011522481.3:c.*17G>A XP_011520783.1:n.*17G>A
XM_017023212.1:c.*17G>A XP_016878701.1:n.*17G>A
XM_024450261.1:c.*17G>A XP_024306029.1:n.*17G>A
NM_001171.6:c.*17G>A MANE Select NP_001162.5:n.*17G>A