Canonical Allele Identifier: CA425567521

Gene: SRD5A2

Linked Data

• MyVariant Identifiers: chr2:g.31756460G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31531390G>A , CM000664.2:g.31531390G>A	GRCh38
NC_000002.11:g.31756460G>A , CM000664.1:g.31756460G>A	GRCh37
NC_000002.10:g.31609964G>A	NCBI36
NG_008365.1:g.54582C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.528C>T MANE Select	ENSP00000477587.1:p.Ile176=
ENST00000622030.1:c.528C>T	ENSP00000477587.1:p.Ile176=
NM_000348.3:c.528C>T	NP_000339.2:p.Ile176=
XM_011533069.1:c.306C>T	XP_011531371.1:p.Ile102=
XM_011533070.1:c.273C>T	XP_011531372.1:p.Ile91=
XM_011533071.1:c.273C>T	XP_011531373.1:p.Ile91=
XM_011533072.1:c.273C>T	XP_011531374.1:p.Ile91=
XM_011533069.2:c.306C>T	XP_011531371.1:p.Ile102=
XM_011533072.2:c.273C>T	XP_011531374.1:p.Ile91=
NM_000348.4:c.528C>T MANE Select	NP_000339.2:p.Ile176=