Canonical Allele Identifier: CA346598392

Gene: SRD5A2

Linked Data

• dbSNP Id: rs1665906434
• gnomAD v4: 2-31531474-T-G
• MyVariant Identifiers: chr2:g.31756544T>G (hg19) ; chr2:g.31531474T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31531474T>G , CM000664.2:g.31531474T>G	GRCh38
NC_000002.11:g.31756544T>G , CM000664.1:g.31756544T>G	GRCh37
NC_000002.10:g.31610048T>G	NCBI36
NG_008365.1:g.54498A>C

Transcript Alleles

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