Canonical Allele Identifier: CA378117643

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101578580A>T (hg19) ; chr10:g.99818823A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99818823A>T , CM000672.2:g.99818823A>T	GRCh38
NC_000010.10:g.101578580A>T , CM000672.1:g.101578580A>T	GRCh37
NC_000010.9:g.101568570A>T	NCBI36
NG_011798.1:g.41118A>T
NG_011798.2:g.41226A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2305A>T MANE Select	ENSP00000497274.1:p.Ile769Phe
ENST00000370449.8:c.2305A>T	ENSP00000359478.4:p.Ile769Phe
NM_000392.4:c.2305A>T	NP_000383.1:p.Ile769Phe
XM_006717630.2:c.1609A>T	XP_006717693.1:p.Ile537Phe
XM_006717631.2:c.2305A>T	XP_006717694.1:p.Ile769Phe
XM_011539291.1:c.2305A>T	XP_011537593.1:p.Ile769Phe
XR_945604.1:n.2494A>T
XR_945605.1:n.2496A>T
NM_000392.5:c.2305A>T MANE Select	NP_000383.2:p.Ile769Phe
XM_006717630.3:c.1609A>T	XP_006717693.1:p.Ile537Phe
XM_006717631.4:c.2305A>T	XP_006717694.1:p.Ile769Phe
XM_011539291.3:c.2305A>T	XP_011537593.1:p.Ile769Phe
XM_017015675.2:c.2305A>T	XP_016871164.1:p.Ile769Phe
XR_945604.3:n.2548A>T
XR_945605.3:n.2548A>T