Canonical Allele Identifier: CA378128538

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101605534C>G (hg19) ; chr10:g.99845777C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845777C>G , CM000672.2:g.99845777C>G	GRCh38
NC_000010.10:g.101605534C>G , CM000672.1:g.101605534C>G	GRCh37
NC_000010.9:g.101595524C>G	NCBI36
NG_011798.1:g.68072C>G
NG_011798.2:g.68180C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4141C>G MANE Select	ENSP00000497274.1:p.Pro1381Ala
ENST00000648523.1:c.29C>G
ENST00000649459.1:n.489C>G
ENST00000370449.8:c.4141C>G	ENSP00000359478.4:p.Pro1381Ala
NM_000392.4:c.4141C>G	NP_000383.1:p.Pro1381Ala
XM_006717630.2:c.3445C>G	XP_006717693.1:p.Pro1149Ala
XR_945604.1:n.4271C>G
XR_945605.1:n.4205C>G
NM_000392.5:c.4141C>G MANE Select	NP_000383.2:p.Pro1381Ala
XM_006717630.3:c.3445C>G	XP_006717693.1:p.Pro1149Ala
XR_945604.3:n.4325C>G
XR_945605.3:n.4257C>G