Canonical Allele Identifier: CA425566442

Gene: SRD5A2

Linked Data

• MyVariant Identifiers: chr2:g.31751202T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526132T>G , CM000664.2:g.31526132T>G	GRCh38
NC_000002.11:g.31751202T>G , CM000664.1:g.31751202T>G	GRCh37
NC_000002.10:g.31604706T>G	NCBI36
NG_008365.1:g.59840A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.*64A>C MANE Select	ENSP00000477587.1:n.*64A>C
ENST00000622030.1:c.*64A>C	ENSP00000477587.1:n.*64A>C
NM_000348.3:c.*64A>C	NP_000339.2:n.*64A>C
XM_011533069.1:c.*64A>C	XP_011531371.1:n.*64A>C
XM_011533070.1:c.*64A>C	XP_011531372.1:n.*64A>C
XM_011533071.1:c.*64A>C	XP_011531373.1:n.*64A>C
XM_011533072.1:c.*64A>C	XP_011531374.1:n.*64A>C
XM_011533069.2:c.*64A>C	XP_011531371.1:n.*64A>C
XM_011533072.2:c.*64A>C	XP_011531374.1:n.*64A>C
NM_000348.4:c.*64A>C MANE Select	NP_000339.2:n.*64A>C