Canonical Allele Identifier: CA1599923

Gene: SRD5A2

Linked Data

• dbSNP Id: rs777907647
• ExAC: 2:31756491 A / G
• gnomAD v2: 2-31756491-A-G
• gnomAD v3: 2-31531421-A-G
• gnomAD v4: 2-31531421-A-G
• MyVariant Identifiers: chr2:g.31756491A>G (hg19) ; chr2:g.31531421A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31531421A>G , CM000664.2:g.31531421A>G	GRCh38
NC_000002.11:g.31756491A>G , CM000664.1:g.31756491A>G	GRCh37
NC_000002.10:g.31609995A>G	NCBI36
NG_008365.1:g.54551T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.497T>C MANE Select	ENSP00000477587.1:p.Ile166Thr
ENST00000622030.1:c.497T>C	ENSP00000477587.1:p.Ile166Thr
NM_000348.3:c.497T>C	NP_000339.2:p.Ile166Thr
XM_011533069.1:c.275T>C	XP_011531371.1:p.Ile92Thr
XM_011533070.1:c.242T>C	XP_011531372.1:p.Ile81Thr
XM_011533071.1:c.242T>C	XP_011531373.1:p.Ile81Thr
XM_011533072.1:c.242T>C	XP_011531374.1:p.Ile81Thr
XM_011533069.2:c.275T>C	XP_011531371.1:p.Ile92Thr
XM_011533072.2:c.242T>C	XP_011531374.1:p.Ile81Thr
NM_000348.4:c.497T>C MANE Select	NP_000339.2:p.Ile166Thr