Canonical Allele Identifier: CA278636388

Gene: ABCC6

Linked Data

• dbSNP Id: rs906122272
• gnomAD v2: 16-16263705-C-G
• gnomAD v4: 16-16169848-C-G
• MyVariant Identifiers: chr16:g.16263705C>G (hg19) ; chr16:g.16169848C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169848C>G , CM000678.2:g.16169848C>G	GRCh38
NC_000016.9:g.16263705C>G , CM000678.1:g.16263705C>G	GRCh37
NC_000016.8:g.16171206C>G	NCBI36
NG_007558.2:g.58624G>C
NG_007558.3:g.58770G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2793G>C	ENSP00000483331.2:p.Lys931Asn
ENST00000205557.12:c.2793G>C MANE Select	ENSP00000205557.7:p.Lys931Asn
ENST00000205557.11:c.2793G>C	ENSP00000205557.7:p.Lys931Asn
ENST00000456970.6:c.2618G>C	ENSP00000405002.2:n.2618G>C
ENST00000622290.4:c.*2G>C	ENSP00000483331.1:n.*2G>C
NM_001171.5:c.2793G>C	NP_001162.4:p.Lys931Asn
XM_011522479.1:c.2760G>C	XP_011520781.1:p.Lys920Asn
XM_011522480.1:c.2451G>C	XP_011520782.1:p.Lys817Asn
XM_011522481.1:c.2451G>C	XP_011520783.1:p.Lys817Asn
XR_932836.1:n.3028G>C
XR_932837.1:n.3029G>C
XR_932838.1:n.3029G>C
NM_001351800.1:c.2451G>C	NP_001338729.1:p.Lys817Asn
NR_147784.1:n.2655G>C
XM_011522479.2:c.2760G>C	XP_011520781.1:p.Lys920Asn
XM_011522481.3:c.2451G>C	XP_011520783.1:p.Lys817Asn
XM_017023212.1:c.2625G>C	XP_016878701.1:p.Lys875Asn
XM_017023214.1:c.2793G>C	XP_016878703.1:p.Lys931Asn
XM_024450261.1:c.2829G>C	XP_024306029.1:p.Lys943Asn
XR_932836.2:n.2974G>C
XR_932837.3:n.2974G>C
XR_932838.3:n.2974G>C
NM_001171.6:c.2793G>C MANE Select	NP_001162.5:p.Lys931Asn