Canonical Allele Identifier: CA2576929396
Gene: SRD5A2 HGNC NCBI

Linked Data

gnomAD v4: 2-31531549-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31531549A>G , CM000664.2:g.31531549A>G GRCh38
NC_000002.11:g.31756619A>G , CM000664.1:g.31756619A>G GRCh37
NC_000002.10:g.31610123A>G NCBI36
NG_008365.1:g.54423T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.446-77T>C MANE Select ENSP00000477587.1:n.446-77T>C
ENST00000622030.1:c.446-77T>C ENSP00000477587.1:n.446-77T>C
NM_000348.3:c.446-77T>C NP_000339.2:n.446-77T>C
XM_011533069.1:c.224-77T>C XP_011531371.1:n.224-77T>C
XM_011533070.1:c.191-77T>C XP_011531372.1:n.191-77T>C
XM_011533071.1:c.191-77T>C XP_011531373.1:n.191-77T>C
XM_011533072.1:c.191-77T>C XP_011531374.1:n.191-77T>C
XM_011533069.2:c.224-77T>C XP_011531371.1:n.224-77T>C
XM_011533072.2:c.191-77T>C XP_011531374.1:n.191-77T>C
NM_000348.4:c.446-77T>C MANE Select NP_000339.2:n.446-77T>C