Canonical Allele Identifier: CA394884925

Gene: ABCC6

Linked Data

• dbSNP Id: rs1422112874
• gnomAD v2: 16-16263659-A-G
• gnomAD v4: 16-16169802-A-G
• MyVariant Identifiers: chr16:g.16263659A>G (hg19) ; chr16:g.16169802A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169802A>G , CM000678.2:g.16169802A>G	GRCh38
NC_000016.9:g.16263659A>G , CM000678.1:g.16263659A>G	GRCh37
NC_000016.8:g.16171160A>G	NCBI36
NG_007558.2:g.58670T>C
NG_007558.3:g.58816T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2839T>C	ENSP00000483331.2:p.Cys947Arg
ENST00000205557.12:c.2839T>C MANE Select	ENSP00000205557.7:p.Cys947Arg
ENST00000205557.11:c.2839T>C	ENSP00000205557.7:p.Cys947Arg
ENST00000456970.6:c.2664T>C	ENSP00000405002.2:n.2664T>C
ENST00000622290.4:c.*48T>C	ENSP00000483331.1:n.*48T>C
NM_001171.5:c.2839T>C	NP_001162.4:p.Cys947Arg
XM_011522479.1:c.2806T>C	XP_011520781.1:p.Cys936Arg
XM_011522480.1:c.2497T>C	XP_011520782.1:p.Cys833Arg
XM_011522481.1:c.2497T>C	XP_011520783.1:p.Cys833Arg
XR_932836.1:n.3074T>C
XR_932837.1:n.3075T>C
XR_932838.1:n.3075T>C
NM_001351800.1:c.2497T>C	NP_001338729.1:p.Cys833Arg
NR_147784.1:n.2701T>C
XM_011522479.2:c.2806T>C	XP_011520781.1:p.Cys936Arg
XM_011522481.3:c.2497T>C	XP_011520783.1:p.Cys833Arg
XM_017023212.1:c.2671T>C	XP_016878701.1:p.Cys891Arg
XM_017023214.1:c.2839T>C	XP_016878703.1:p.Cys947Arg
XM_024450261.1:c.2875T>C	XP_024306029.1:p.Cys959Arg
XR_932836.2:n.3020T>C
XR_932837.3:n.3020T>C
XR_932838.3:n.3020T>C
NM_001171.6:c.2839T>C MANE Select	NP_001162.5:p.Cys947Arg