Canonical Allele Identifier: CA2631959810
Gene: ABCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155251A>G , CM000678.2:g.16155251A>G GRCh38
NC_000016.9:g.16249108A>G , CM000678.1:g.16249108A>G GRCh37
NC_000016.8:g.16156609A>G NCBI36
NG_007558.2:g.73221T>C
NG_007558.3:g.73367T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.526T>C
ENST00000622290.5:c.*55-220T>C ENSP00000483331.2:n.*55-220T>C
ENST00000205557.12:c.3883-220T>C MANE Select ENSP00000205557.7:n.3883-220T>C
ENST00000640696.1:c.697-220T>C ENSP00000492197.1:n.697-220T>C
ENST00000205557.11:c.3883-220T>C ENSP00000205557.7:n.3883-220T>C
ENST00000456970.6:c.3508-220T>C ENSP00000405002.2:n.3508-220T>C
ENST00000576204.5:n.526T>C
ENST00000622290.4:c.*1092-220T>C ENSP00000483331.1:n.*1092-220T>C
NM_001171.5:c.3883-220T>C NP_001162.4:n.3883-220T>C
XM_011522479.1:c.3850-220T>C XP_011520781.1:n.3850-220T>C
XM_011522480.1:c.3541-220T>C XP_011520782.1:n.3541-220T>C
XM_011522481.1:c.3541-220T>C XP_011520783.1:n.3541-220T>C
XR_932836.1:n.4181-220T>C
XR_932837.1:n.3919-220T>C
XR_932838.1:n.3982-220T>C
XR_933134.1:n.539-4530A>G
NM_001351800.1:c.3541-220T>C NP_001338729.1:n.3541-220T>C
NR_147784.1:n.3545-220T>C
XM_011522479.2:c.3850-220T>C XP_011520781.1:n.3850-220T>C
XM_011522481.3:c.3541-220T>C XP_011520783.1:n.3541-220T>C
XM_017023212.1:c.3715-220T>C XP_016878701.1:n.3715-220T>C
XM_024450261.1:c.3919-220T>C XP_024306029.1:n.3919-220T>C
XR_932836.2:n.4127-220T>C
XR_932837.3:n.3864-220T>C
XR_932838.3:n.3927-220T>C
NM_001171.6:c.3883-220T>C MANE Select NP_001162.5:n.3883-220T>C