Canonical Allele Identifier: CA2533108731
Gene: SRD5A2 HGNC NCBI

Linked Data

gnomAD v4: 2-31531353-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31531353G>A , CM000664.2:g.31531353G>A GRCh38
NC_000002.11:g.31756423G>A , CM000664.1:g.31756423G>A GRCh37
NC_000002.10:g.31609927G>A NCBI36
NG_008365.1:g.54619C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.547+18C>T MANE Select ENSP00000477587.1:n.547+18C>T
ENST00000622030.1:c.547+18C>T ENSP00000477587.1:n.547+18C>T
NM_000348.3:c.547+18C>T NP_000339.2:n.547+18C>T
XM_011533069.1:c.325+18C>T XP_011531371.1:n.325+18C>T
XM_011533070.1:c.292+18C>T XP_011531372.1:n.292+18C>T
XM_011533071.1:c.292+18C>T XP_011531373.1:n.292+18C>T
XM_011533072.1:c.292+18C>T XP_011531374.1:n.292+18C>T
XM_011533069.2:c.325+18C>T XP_011531371.1:n.325+18C>T
XM_011533072.2:c.292+18C>T XP_011531374.1:n.292+18C>T
NM_000348.4:c.547+18C>T MANE Select NP_000339.2:n.547+18C>T