Canonical Allele Identifier: CA2838622953
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16163201G>T , CM000678.2:g.16163201G>T GRCh38
NC_000016.9:g.16257058G>T , CM000678.1:g.16257058G>T GRCh37
NC_000016.8:g.16164559G>T NCBI36
NG_007558.2:g.65271C>A
NG_007558.3:g.65417C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.3307-9C>A ENSP00000483331.2:n.3307-9C>A
ENST00000205557.12:c.3307-9C>A MANE Select ENSP00000205557.7:n.3307-9C>A
ENST00000640696.1:c.321-1637C>A ENSP00000492197.1:n.321-1637C>A
ENST00000205557.11:c.3307-9C>A ENSP00000205557.7:n.3307-9C>A
ENST00000456970.6:c.3132-1637C>A ENSP00000405002.2:n.3132-1637C>A
ENST00000622290.4:c.*516-9C>A ENSP00000483331.1:n.*516-9C>A
NM_001171.5:c.3307-9C>A NP_001162.4:n.3307-9C>A
XM_011522479.1:c.3274-9C>A XP_011520781.1:n.3274-9C>A
XM_011522480.1:c.2965-9C>A XP_011520782.1:n.2965-9C>A
XM_011522481.1:c.2965-9C>A XP_011520783.1:n.2965-9C>A
XR_932836.1:n.3542-9C>A
XR_932837.1:n.3543-1637C>A
XR_932838.1:n.3543-1637C>A
XR_933133.1:n.407+358G>T
XR_933134.1:n.754+358G>T
NM_001351800.1:c.2965-9C>A NP_001338729.1:n.2965-9C>A
NR_147784.1:n.3169-1637C>A
XM_011522479.2:c.3274-9C>A XP_011520781.1:n.3274-9C>A
XM_011522481.3:c.2965-9C>A XP_011520783.1:n.2965-9C>A
XM_017023212.1:c.3139-9C>A XP_016878701.1:n.3139-9C>A
XM_017023214.1:c.3307-1637C>A XP_016878703.1:n.3307-1637C>A
XM_024450261.1:c.3343-9C>A XP_024306029.1:n.3343-9C>A
XR_932836.2:n.3488-9C>A
XR_932837.3:n.3488-1637C>A
XR_932838.3:n.3488-1637C>A
NM_001171.6:c.3307-9C>A MANE Select NP_001162.5:n.3307-9C>A