Canonical Allele Identifier: CA4494155

Gene: AKR1B15

Linked Data

• dbSNP Id: rs4732038
• ExAC: 7:134250322 A / C
• gnomAD v2: 7-134250322-A-C
• gnomAD v3: 7-134565570-A-C
• gnomAD v4: 7-134565570-A-C
• MyVariant Identifiers: chr7:g.134250322A>C (hg19) ; chr7:g.134565570A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.134565570A>C , CM000669.2:g.134565570A>C	GRCh38
NC_000007.13:g.134250322A>C , CM000669.1:g.134250322A>C	GRCh37
NC_000007.12:g.133900862A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000457545.7:c.150+801A>C MANE Select	ENSP00000389289.1:n.150+801A>C
ENST00000652743.1:c.66+24A>C	ENSP00000498877.1:n.66+24A>C
ENST00000423958.2:c.150+801A>C	ENSP00000397009.2:n.150+801A>C
ENST00000457545.6:c.150+801A>C	ENSP00000389289.1:n.150+801A>C
ENST00000467156.1:n.759+24A>C
NM_001080538.2:c.150+801A>C	NP_001074007.2:n.150+801A>C
XM_011516240.1:c.150+801A>C	XP_011514542.1:n.150+801A>C
XM_011516241.1:c.66+24A>C	XP_011514543.1:n.66+24A>C
XM_011516242.1:c.150+801A>C	XP_011514544.1:n.150+801A>C
XM_011516241.3:c.66+24A>C	XP_011514543.2:n.66+24A>C
XM_017012224.2:c.150+801A>C	XP_016867713.1:n.150+801A>C
NM_001080538.3:c.150+801A>C MANE Select	NP_001074007.2:n.150+801A>C
NM_001367820.1:c.150+801A>C	NP_001354749.1:n.150+801A>C
NM_001367821.1:c.66+24A>C	NP_001354750.1:n.66+24A>C
NM_001367822.1:c.150+801A>C	NP_001354751.1:n.150+801A>C
NR_160301.1:n.1089+24A>C
NR_160302.1:n.141-2588A>C