Canonical Allele Identifier: CA471128867

Gene: ABCC2

Linked Data

• dbSNP Id: rs1713582299
• gnomAD v4: 10-99811540-A-G
• MyVariant Identifiers: chr10:g.101571297A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99811540A>G , CM000672.2:g.99811540A>G	GRCh38
NC_000010.10:g.101571297A>G , CM000672.1:g.101571297A>G	GRCh37
NC_000010.9:g.101561287A>G	NCBI36
NG_011798.1:g.33835A>G
NG_011798.2:g.33943A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.1905A>G MANE Select	ENSP00000497274.1:p.Lys635=
ENST00000370449.8:c.1905A>G	ENSP00000359478.4:p.Lys635=
NM_000392.4:c.1905A>G	NP_000383.1:p.Lys635=
XM_006717630.2:c.1209A>G	XP_006717693.1:p.Lys403=
XM_006717631.2:c.1905A>G	XP_006717694.1:p.Lys635=
XM_011539291.1:c.1905A>G	XP_011537593.1:p.Lys635=
XR_945604.1:n.2094A>G
XR_945605.1:n.2096A>G
NM_000392.5:c.1905A>G MANE Select	NP_000383.2:p.Lys635=
XM_006717630.3:c.1209A>G	XP_006717693.1:p.Lys403=
XM_006717631.4:c.1905A>G	XP_006717694.1:p.Lys635=
XM_011539291.3:c.1905A>G	XP_011537593.1:p.Lys635=
XM_017015675.2:c.1905A>G	XP_016871164.1:p.Lys635=
XR_945604.3:n.2148A>G
XR_945605.3:n.2148A>G