Canonical Allele Identifier: CA425559908

Gene: SRD5A2

Linked Data

• gnomAD v4: 2-31523875-C-A
• MyVariant Identifiers: chr2:g.31748945C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31523875C>A , CM000664.2:g.31523875C>A	GRCh38
NC_000002.11:g.31748945C>A , CM000664.1:g.31748945C>A	GRCh37
NC_000002.10:g.31602449C>A	NCBI36
NG_008365.1:g.62097G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.*2321G>T MANE Select	ENSP00000477587.1:n.*2321G>T
ENST00000622030.1:c.*2321G>T	ENSP00000477587.1:n.*2321G>T
XM_011533069.1:c.*2321G>T	XP_011531371.1:n.*2321G>T
XM_011533070.1:c.*2321G>T	XP_011531372.1:n.*2321G>T
XM_011533071.1:c.*2321G>T	XP_011531373.1:n.*2321G>T
XM_011533072.1:c.*2321G>T	XP_011531374.1:n.*2321G>T
XM_011533069.2:c.*2321G>T	XP_011531371.1:n.*2321G>T
XM_011533072.2:c.*2321G>T	XP_011531374.1:n.*2321G>T
NM_000348.4:c.*2321G>T MANE Select	NP_000339.2:n.*2321G>T