Canonical Allele Identifier: CA2210133530

Gene: ABCC6

Linked Data

• dbSNP Id: rs2046341005
• gnomAD v4: 16-16149915-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16149915G>C , CM000678.2:g.16149915G>C	GRCh38
NC_000016.9:g.16243772G>C , CM000678.1:g.16243772G>C	GRCh37
NC_000016.8:g.16151273G>C	NCBI36
NG_007558.2:g.78557C>G
NG_007558.3:g.78703C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*902C>G	ENSP00000483331.2:n.*902C>G
ENST00000205557.12:c.*218C>G MANE Select	ENSP00000205557.7:n.*218C>G
ENST00000640696.1:c.1544C>G	ENSP00000492197.1:n.1544C>G
ENST00000205557.11:c.*218C>G	ENSP00000205557.7:n.*218C>G
ENST00000576204.5:n.1593C>G
ENST00000622290.4:c.*1939C>G	ENSP00000483331.1:n.*1939C>G
NM_001171.5:c.*218C>G	NP_001162.4:n.*218C>G
XM_011522479.1:c.*218C>G	XP_011520781.1:n.*218C>G
XM_011522480.1:c.*218C>G	XP_011520782.1:n.*218C>G
XM_011522481.1:c.*218C>G	XP_011520783.1:n.*218C>G
XR_933134.1:n.538+5625G>C
NM_001351800.1:c.*218C>G	NP_001338729.1:n.*218C>G
NR_147784.1:n.4392C>G
XM_011522479.2:c.*218C>G	XP_011520781.1:n.*218C>G
XM_011522481.3:c.*218C>G	XP_011520783.1:n.*218C>G
XM_017023212.1:c.*218C>G	XP_016878701.1:n.*218C>G
XM_024450261.1:c.*218C>G	XP_024306029.1:n.*218C>G
NM_001171.6:c.*218C>G MANE Select	NP_001162.5:n.*218C>G