Canonical Allele Identifier: CA2658497393

Gene: SRD5A2

Linked Data

• gnomAD v4: 2-31526346-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526346A>G , CM000664.2:g.31526346A>G	GRCh38
NC_000002.11:g.31751416A>G , CM000664.1:g.31751416A>G	GRCh37
NC_000002.10:g.31604920A>G	NCBI36
NG_008365.1:g.59626T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.699-84T>C MANE Select	ENSP00000477587.1:n.699-84T>C
ENST00000622030.1:c.699-84T>C	ENSP00000477587.1:n.699-84T>C
NM_000348.3:c.699-84T>C	NP_000339.2:n.699-84T>C
XM_011533069.1:c.477-84T>C	XP_011531371.1:n.477-84T>C
XM_011533070.1:c.444-84T>C	XP_011531372.1:n.444-84T>C
XM_011533071.1:c.444-84T>C	XP_011531373.1:n.444-84T>C
XM_011533072.1:c.444-84T>C	XP_011531374.1:n.444-84T>C
XM_011533069.2:c.477-84T>C	XP_011531371.1:n.477-84T>C
XM_011533072.2:c.444-84T>C	XP_011531374.1:n.444-84T>C
NM_000348.4:c.699-84T>C MANE Select	NP_000339.2:n.699-84T>C