Canonical Allele Identifier: CA425566534

Gene: SRD5A2

Linked Data

• gnomAD v4: 2-31526166-G-T
• MyVariant Identifiers: chr2:g.31751236G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526166G>T , CM000664.2:g.31526166G>T	GRCh38
NC_000002.11:g.31751236G>T , CM000664.1:g.31751236G>T	GRCh37
NC_000002.10:g.31604740G>T	NCBI36
NG_008365.1:g.59806C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.*30C>A MANE Select	ENSP00000477587.1:n.*30C>A
ENST00000622030.1:c.*30C>A	ENSP00000477587.1:n.*30C>A
NM_000348.3:c.*30C>A	NP_000339.2:n.*30C>A
XM_011533069.1:c.*30C>A	XP_011531371.1:n.*30C>A
XM_011533070.1:c.*30C>A	XP_011531372.1:n.*30C>A
XM_011533071.1:c.*30C>A	XP_011531373.1:n.*30C>A
XM_011533072.1:c.*30C>A	XP_011531374.1:n.*30C>A
XM_011533069.2:c.*30C>A	XP_011531371.1:n.*30C>A
XM_011533072.2:c.*30C>A	XP_011531374.1:n.*30C>A
NM_000348.4:c.*30C>A MANE Select	NP_000339.2:n.*30C>A