Canonical Allele Identifier: CA425627712
Gene: SRD5A2 HGNC NCBI

Linked Data

gnomAD v4: 2-31580973-C-G
MyVariant Identifiers: chr2:g.31806042C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31580973C>G , CM000664.2:g.31580973C>G GRCh38
NC_000002.11:g.31806042C>G , CM000664.1:g.31806042C>G GRCh37
NC_000002.10:g.31659546C>G NCBI36
NG_008365.1:g.4999G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.1:c.-73G>C ENSP00000477587.1:n.-73G>C
XM_011533068.1:c.-73G>C XP_011531370.1:n.-73G>C
XM_011533070.1:c.27-47207G>C XP_011531372.1:n.27-47207G>C
XM_011533071.1:c.27-47207G>C XP_011531373.1:n.27-47207G>C
XM_011533072.1:c.27-47207G>C XP_011531374.1:n.27-47207G>C
XM_011533072.2:c.27-47207G>C XP_011531374.1:n.27-47207G>C