Canonical Allele Identifier: CA2658498772

Gene: SRD5A2

Linked Data

• gnomAD v4: 2-31531520-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31531520A>C , CM000664.2:g.31531520A>C	GRCh38
NC_000002.11:g.31756590A>C , CM000664.1:g.31756590A>C	GRCh37
NC_000002.10:g.31610094A>C	NCBI36
NG_008365.1:g.54452T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.446-48T>G MANE Select	ENSP00000477587.1:n.446-48T>G
ENST00000622030.1:c.446-48T>G	ENSP00000477587.1:n.446-48T>G
NM_000348.3:c.446-48T>G	NP_000339.2:n.446-48T>G
XM_011533069.1:c.224-48T>G	XP_011531371.1:n.224-48T>G
XM_011533070.1:c.191-48T>G	XP_011531372.1:n.191-48T>G
XM_011533071.1:c.191-48T>G	XP_011531373.1:n.191-48T>G
XM_011533072.1:c.191-48T>G	XP_011531374.1:n.191-48T>G
XM_011533069.2:c.224-48T>G	XP_011531371.1:n.224-48T>G
XM_011533072.2:c.191-48T>G	XP_011531374.1:n.191-48T>G
NM_000348.4:c.446-48T>G MANE Select	NP_000339.2:n.446-48T>G