Canonical Allele Identifier: CA394884292

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16169675-C-G
• MyVariant Identifiers: chr16:g.16263532C>G (hg19) ; chr16:g.16169675C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169675C>G , CM000678.2:g.16169675C>G	GRCh38
NC_000016.9:g.16263532C>G , CM000678.1:g.16263532C>G	GRCh37
NC_000016.8:g.16171033C>G	NCBI36
NG_007558.2:g.58797G>C
NG_007558.3:g.58943G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2966G>C	ENSP00000483331.2:p.Gly989Ala
ENST00000205557.12:c.2966G>C MANE Select	ENSP00000205557.7:p.Gly989Ala
ENST00000205557.11:c.2966G>C	ENSP00000205557.7:p.Gly989Ala
ENST00000456970.6:c.2791G>C	ENSP00000405002.2:n.2791G>C
ENST00000622290.4:c.*175G>C	ENSP00000483331.1:n.*175G>C
NM_001171.5:c.2966G>C	NP_001162.4:p.Gly989Ala
XM_011522479.1:c.2933G>C	XP_011520781.1:p.Gly978Ala
XM_011522480.1:c.2624G>C	XP_011520782.1:p.Gly875Ala
XM_011522481.1:c.2624G>C	XP_011520783.1:p.Gly875Ala
XR_932836.1:n.3201G>C
XR_932837.1:n.3202G>C
XR_932838.1:n.3202G>C
NM_001351800.1:c.2624G>C	NP_001338729.1:p.Gly875Ala
NR_147784.1:n.2828G>C
XM_011522479.2:c.2933G>C	XP_011520781.1:p.Gly978Ala
XM_011522481.3:c.2624G>C	XP_011520783.1:p.Gly875Ala
XM_017023212.1:c.2798G>C	XP_016878701.1:p.Gly933Ala
XM_017023214.1:c.2966G>C	XP_016878703.1:p.Gly989Ala
XM_024450261.1:c.3002G>C	XP_024306029.1:p.Gly1001Ala
XR_932836.2:n.3147G>C
XR_932837.3:n.3147G>C
XR_932838.3:n.3147G>C
NM_001171.6:c.2966G>C MANE Select	NP_001162.5:p.Gly989Ala