Canonical Allele Identifier: CA493799334

Gene: ABCC6

Linked Data

• ClinVar Variation Id: 1656201
• ClinVar RCV Id: RCV002161619
• dbSNP Id: rs1240073394
• gnomAD v2: 16-16263522-C-G
• gnomAD v3: 16-16169665-C-G
• gnomAD v4: 16-16169665-C-G
• MyVariant Identifiers: chr16:g.16263522C>G (hg19) ; chr16:g.16169665C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169665C>G , CM000678.2:g.16169665C>G	GRCh38
NC_000016.9:g.16263522C>G , CM000678.1:g.16263522C>G	GRCh37
NC_000016.8:g.16171023C>G	NCBI36
NG_007558.2:g.58807G>C
NG_007558.3:g.58953G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2976G>C	ENSP00000483331.2:p.Gly992=
ENST00000205557.12:c.2976G>C MANE Select	ENSP00000205557.7:p.Gly992=
ENST00000205557.11:c.2976G>C	ENSP00000205557.7:p.Gly992=
ENST00000456970.6:c.2801G>C	ENSP00000405002.2:n.2801G>C
ENST00000622290.4:c.*185G>C	ENSP00000483331.1:n.*185G>C
NM_001171.5:c.2976G>C	NP_001162.4:p.Gly992=
XM_011522479.1:c.2943G>C	XP_011520781.1:p.Gly981=
XM_011522480.1:c.2634G>C	XP_011520782.1:p.Gly878=
XM_011522481.1:c.2634G>C	XP_011520783.1:p.Gly878=
XR_932836.1:n.3211G>C
XR_932837.1:n.3212G>C
XR_932838.1:n.3212G>C
NM_001351800.1:c.2634G>C	NP_001338729.1:p.Gly878=
NR_147784.1:n.2838G>C
XM_011522479.2:c.2943G>C	XP_011520781.1:p.Gly981=
XM_011522481.3:c.2634G>C	XP_011520783.1:p.Gly878=
XM_017023212.1:c.2808G>C	XP_016878701.1:p.Gly936=
XM_017023214.1:c.2976G>C	XP_016878703.1:p.Gly992=
XM_024450261.1:c.3012G>C	XP_024306029.1:p.Gly1004=
XR_932836.2:n.3157G>C
XR_932837.3:n.3157G>C
XR_932838.3:n.3157G>C
NM_001171.6:c.2976G>C MANE Select	NP_001162.5:p.Gly992=