Canonical Allele Identifier: CA2210137179
Gene: ABCC6 HGNC NCBI

Linked Data

dbSNP Id: rs2046783204

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16163250T>G , CM000678.2:g.16163250T>G GRCh38
NC_000016.9:g.16257107T>G , CM000678.1:g.16257107T>G GRCh37
NC_000016.8:g.16164608T>G NCBI36
NG_007558.2:g.65222A>C
NG_007558.3:g.65368A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.3307-58A>C ENSP00000483331.2:n.3307-58A>C
ENST00000205557.12:c.3307-58A>C MANE Select ENSP00000205557.7:n.3307-58A>C
ENST00000640696.1:c.321-1686A>C ENSP00000492197.1:n.321-1686A>C
ENST00000205557.11:c.3307-58A>C ENSP00000205557.7:n.3307-58A>C
ENST00000456970.6:c.3132-1686A>C ENSP00000405002.2:n.3132-1686A>C
ENST00000622290.4:c.*516-58A>C ENSP00000483331.1:n.*516-58A>C
NM_001171.5:c.3307-58A>C NP_001162.4:n.3307-58A>C
XM_011522479.1:c.3274-58A>C XP_011520781.1:n.3274-58A>C
XM_011522480.1:c.2965-58A>C XP_011520782.1:n.2965-58A>C
XM_011522481.1:c.2965-58A>C XP_011520783.1:n.2965-58A>C
XR_932836.1:n.3542-58A>C
XR_932837.1:n.3543-1686A>C
XR_932838.1:n.3543-1686A>C
XR_933133.1:n.407+407T>G
XR_933134.1:n.754+407T>G
NM_001351800.1:c.2965-58A>C NP_001338729.1:n.2965-58A>C
NR_147784.1:n.3169-1686A>C
XM_011522479.2:c.3274-58A>C XP_011520781.1:n.3274-58A>C
XM_011522481.3:c.2965-58A>C XP_011520783.1:n.2965-58A>C
XM_017023212.1:c.3139-58A>C XP_016878701.1:n.3139-58A>C
XM_017023214.1:c.3307-1686A>C XP_016878703.1:n.3307-1686A>C
XM_024450261.1:c.3343-58A>C XP_024306029.1:n.3343-58A>C
XR_932836.2:n.3488-58A>C
XR_932837.3:n.3488-1686A>C
XR_932838.3:n.3488-1686A>C
NM_001171.6:c.3307-58A>C MANE Select NP_001162.5:n.3307-58A>C