Canonical Allele Identifier: CA212867112

Gene: ABCC2

Linked Data

• dbSNP Id: rs376321366
• gnomAD v2: 10-101604027-C-T
• gnomAD v3: 10-99844270-C-T
• gnomAD v4: 10-99844270-C-T
• MyVariant Identifiers: chr10:g.101604027C>T (hg19) ; chr10:g.99844270C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844270C>T , CM000672.2:g.99844270C>T	GRCh38
NC_000010.10:g.101604027C>T , CM000672.1:g.101604027C>T	GRCh37
NC_000010.9:g.101594017C>T	NCBI36
NG_011798.1:g.66565C>T
NG_011798.2:g.66673C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3844-52C>T MANE Select	ENSP00000497274.1:n.3844-52C>T
ENST00000649459.1:n.192-52C>T
ENST00000370449.8:c.3844-52C>T	ENSP00000359478.4:n.3844-52C>T
NM_000392.4:c.3844-52C>T	NP_000383.1:n.3844-52C>T
XM_006717630.2:c.3148-52C>T	XP_006717693.1:n.3148-52C>T
XR_945604.1:n.4033-52C>T
XR_945605.1:n.3908-52C>T
NM_000392.5:c.3844-52C>T MANE Select	NP_000383.2:n.3844-52C>T
XM_006717630.3:c.3148-52C>T	XP_006717693.1:n.3148-52C>T
XR_945604.3:n.4087-52C>T
XR_945605.3:n.3960-52C>T