Canonical Allele Identifier: CA425627769
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs2148107547
gnomAD v4: 2-31580984-A-C
MyVariant Identifiers: chr2:g.31806053A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31580984A>C , CM000664.2:g.31580984A>C GRCh38
NC_000002.11:g.31806053A>C , CM000664.1:g.31806053A>C GRCh37
NC_000002.10:g.31659557A>C NCBI36
NG_008365.1:g.4988T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.1:c.-84T>G ENSP00000477587.1:n.-84T>G
XM_011533068.1:c.-84T>G XP_011531370.1:n.-84T>G
XM_011533070.1:c.27-47218T>G XP_011531372.1:n.27-47218T>G
XM_011533071.1:c.27-47218T>G XP_011531373.1:n.27-47218T>G
XM_011533072.1:c.27-47218T>G XP_011531374.1:n.27-47218T>G
XM_011533072.2:c.27-47218T>G XP_011531374.1:n.27-47218T>G