Canonical Allele Identifier: CA425627729
Gene: SRD5A2 HGNC NCBI

Linked Data

gnomAD v4: 2-31580976-C-T
MyVariant Identifiers: chr2:g.31806045C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31580976C>T , CM000664.2:g.31580976C>T GRCh38
NC_000002.11:g.31806045C>T , CM000664.1:g.31806045C>T GRCh37
NC_000002.10:g.31659549C>T NCBI36
NG_008365.1:g.4996G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.1:c.-76G>A ENSP00000477587.1:n.-76G>A
XM_011533068.1:c.-76G>A XP_011531370.1:n.-76G>A
XM_011533070.1:c.27-47210G>A XP_011531372.1:n.27-47210G>A
XM_011533071.1:c.27-47210G>A XP_011531373.1:n.27-47210G>A
XM_011533072.1:c.27-47210G>A XP_011531374.1:n.27-47210G>A
XM_011533072.2:c.27-47210G>A XP_011531374.1:n.27-47210G>A
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