Canonical Allele Identifier: CA346598577

Gene: SRD5A2

Linked Data

• MyVariant Identifiers: chr2:g.31758753T>G (hg19) ; chr2:g.31533683T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31533683T>G , CM000664.2:g.31533683T>G	GRCh38
NC_000002.11:g.31758753T>G , CM000664.1:g.31758753T>G	GRCh37
NC_000002.10:g.31612257T>G	NCBI36
NG_008365.1:g.52289A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.365A>C MANE Select	ENSP00000477587.1:p.Asn122Thr
ENST00000622030.1:c.365A>C	ENSP00000477587.1:p.Asn122Thr
NM_000348.3:c.365A>C	NP_000339.2:p.Asn122Thr
XM_011533068.1:c.365A>C	XP_011531370.1:p.Asn122Thr
XM_011533069.1:c.143A>C	XP_011531371.1:p.Asn48Thr
XM_011533070.1:c.110A>C	XP_011531372.1:p.Asn37Thr
XM_011533071.1:c.110A>C	XP_011531373.1:p.Asn37Thr
XM_011533072.1:c.110A>C	XP_011531374.1:p.Asn37Thr
XM_011533069.2:c.143A>C	XP_011531371.1:p.Asn48Thr
XM_011533072.2:c.110A>C	XP_011531374.1:p.Asn37Thr
NM_000348.4:c.365A>C MANE Select	NP_000339.2:p.Asn122Thr