Canonical Allele Identifier: CA7925742

Gene: ABCC6

Linked Data

• dbSNP Id: rs755557398
• ExAC: 16:16263559 T / C
• gnomAD v2: 16-16263559-T-C
• gnomAD v3: 16-16169702-T-C
• gnomAD v4: 16-16169702-T-C
• MyVariant Identifiers: chr16:g.16263559T>C (hg19) ; chr16:g.16169702T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169702T>C , CM000678.2:g.16169702T>C	GRCh38
NC_000016.9:g.16263559T>C , CM000678.1:g.16263559T>C	GRCh37
NC_000016.8:g.16171060T>C	NCBI36
NG_007558.2:g.58770A>G
NG_007558.3:g.58916A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2939A>G	ENSP00000483331.2:p.Gln980Arg
ENST00000205557.12:c.2939A>G MANE Select	ENSP00000205557.7:p.Gln980Arg
ENST00000205557.11:c.2939A>G	ENSP00000205557.7:p.Gln980Arg
ENST00000456970.6:c.2764A>G	ENSP00000405002.2:n.2764A>G
ENST00000622290.4:c.*148A>G	ENSP00000483331.1:n.*148A>G
NM_001171.5:c.2939A>G	NP_001162.4:p.Gln980Arg
XM_011522479.1:c.2906A>G	XP_011520781.1:p.Gln969Arg
XM_011522480.1:c.2597A>G	XP_011520782.1:p.Gln866Arg
XM_011522481.1:c.2597A>G	XP_011520783.1:p.Gln866Arg
XR_932836.1:n.3174A>G
XR_932837.1:n.3175A>G
XR_932838.1:n.3175A>G
NM_001351800.1:c.2597A>G	NP_001338729.1:p.Gln866Arg
NR_147784.1:n.2801A>G
XM_011522479.2:c.2906A>G	XP_011520781.1:p.Gln969Arg
XM_011522481.3:c.2597A>G	XP_011520783.1:p.Gln866Arg
XM_017023212.1:c.2771A>G	XP_016878701.1:p.Gln924Arg
XM_017023214.1:c.2939A>G	XP_016878703.1:p.Gln980Arg
XM_024450261.1:c.2975A>G	XP_024306029.1:p.Gln992Arg
XR_932836.2:n.3120A>G
XR_932837.3:n.3120A>G
XR_932838.3:n.3120A>G
NM_001171.6:c.2939A>G MANE Select	NP_001162.5:p.Gln980Arg