Canonical Allele Identifier: CA5643395

Gene: ABCC2

Linked Data

• dbSNP Id: rs770975345
• ExAC: 10:101577017 C / T
• gnomAD v2: 10-101577017-C-T
• gnomAD v3: 10-99817260-C-T
• gnomAD v4: 10-99817260-C-T
• MyVariant Identifiers: chr10:g.101577017C>T (hg19) ; chr10:g.99817260C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99817260C>T , CM000672.2:g.99817260C>T	GRCh38
NC_000010.10:g.101577017C>T , CM000672.1:g.101577017C>T	GRCh37
NC_000010.9:g.101567007C>T	NCBI36
NG_011798.1:g.39555C>T
NG_011798.2:g.39663C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2095-48C>T MANE Select	ENSP00000497274.1:n.2095-48C>T
ENST00000370449.8:c.2095-48C>T	ENSP00000359478.4:n.2095-48C>T
NM_000392.4:c.2095-48C>T	NP_000383.1:n.2095-48C>T
XM_006717630.2:c.1399-48C>T	XP_006717693.1:n.1399-48C>T
XM_006717631.2:c.2095-48C>T	XP_006717694.1:n.2095-48C>T
XM_011539291.1:c.2095-48C>T	XP_011537593.1:n.2095-48C>T
XR_945604.1:n.2284-48C>T
XR_945605.1:n.2286-48C>T
NM_000392.5:c.2095-48C>T MANE Select	NP_000383.2:n.2095-48C>T
XM_006717630.3:c.1399-48C>T	XP_006717693.1:n.1399-48C>T
XM_006717631.4:c.2095-48C>T	XP_006717694.1:n.2095-48C>T
XM_011539291.3:c.2095-48C>T	XP_011537593.1:n.2095-48C>T
XM_017015675.2:c.2095-48C>T	XP_016871164.1:n.2095-48C>T
XR_945604.3:n.2338-48C>T
XR_945605.3:n.2338-48C>T