Canonical Allele Identifier: CA346598217

Gene: SRD5A2

Linked Data

• gnomAD v4: 2-31531398-C-A
• MyVariant Identifiers: chr2:g.31756468C>A (hg19) ; chr2:g.31531398C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31531398C>A , CM000664.2:g.31531398C>A	GRCh38
NC_000002.11:g.31756468C>A , CM000664.1:g.31756468C>A	GRCh37
NC_000002.10:g.31609972C>A	NCBI36
NG_008365.1:g.54574G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.520G>T MANE Select	ENSP00000477587.1:p.Gly174Ter
ENST00000622030.1:c.520G>T	ENSP00000477587.1:p.Gly174Ter
NM_000348.3:c.520G>T	NP_000339.2:p.Gly174Ter
XM_011533069.1:c.298G>T	XP_011531371.1:p.Gly100Ter
XM_011533070.1:c.265G>T	XP_011531372.1:p.Gly89Ter
XM_011533071.1:c.265G>T	XP_011531373.1:p.Gly89Ter
XM_011533072.1:c.265G>T	XP_011531374.1:p.Gly89Ter
XM_011533069.2:c.298G>T	XP_011531371.1:p.Gly100Ter
XM_011533072.2:c.265G>T	XP_011531374.1:p.Gly89Ter
NM_000348.4:c.520G>T MANE Select	NP_000339.2:p.Gly174Ter