Canonical Allele Identifier: CA595642526

Gene: ABCC2

Linked Data

• dbSNP Id: rs1304108859
• gnomAD v2: 10-101605166-C-T
• gnomAD v3: 10-99845409-C-T
• gnomAD v4: 10-99845409-C-T
• MyVariant Identifiers: chr10:g.101605166C>T (hg19) ; chr10:g.99845409C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845409C>T , CM000672.2:g.99845409C>T	GRCh38
NC_000010.10:g.101605166C>T , CM000672.1:g.101605166C>T	GRCh37
NC_000010.9:g.101595156C>T	NCBI36
NG_011798.1:g.67704C>T
NG_011798.2:g.67812C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3988-215C>T MANE Select	ENSP00000497274.1:n.3988-215C>T
ENST00000649459.1:n.336-215C>T
ENST00000370449.8:c.3988-215C>T	ENSP00000359478.4:n.3988-215C>T
NM_000392.4:c.3988-215C>T	NP_000383.1:n.3988-215C>T
XM_006717630.2:c.3292-215C>T	XP_006717693.1:n.3292-215C>T
XR_945604.1:n.4177-274C>T
XR_945605.1:n.4052-215C>T
NM_000392.5:c.3988-215C>T MANE Select	NP_000383.2:n.3988-215C>T
XM_006717630.3:c.3292-215C>T	XP_006717693.1:n.3292-215C>T
XR_945604.3:n.4231-274C>T
XR_945605.3:n.4104-215C>T