Canonical Allele Identifier: CA1242215105
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1666780895
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31568419G>A , CM000664.2:g.31568419G>A GRCh38
NC_000002.11:g.31793489G>A , CM000664.1:g.31793489G>A GRCh37
NC_000002.10:g.31646993G>A NCBI36
NG_008365.1:g.17553C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.281+12201C>T MANE Select ENSP00000477587.1:n.281+12201C>T
ENST00000622030.1:c.281+12201C>T ENSP00000477587.1:n.281+12201C>T
NM_000348.3:c.281+12201C>T NP_000339.2:n.281+12201C>T
XM_011533068.1:c.281+12201C>T XP_011531370.1:n.281+12201C>T
XM_011533070.1:c.27-34653C>T XP_011531372.1:n.27-34653C>T
XM_011533071.1:c.27-34653C>T XP_011531373.1:n.27-34653C>T
XM_011533072.1:c.27-34653C>T XP_011531374.1:n.27-34653C>T
XM_011533072.2:c.27-34653C>T XP_011531374.1:n.27-34653C>T
NM_000348.4:c.281+12201C>T MANE Select NP_000339.2:n.281+12201C>T
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