Canonical Allele Identifier: CA425566455
Gene: SRD5A2 HGNC NCBI

Linked Data

gnomAD v3: 2-31526137-G-T
gnomAD v4: 2-31526137-G-T
MyVariant Identifiers: chr2:g.31751207G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31526137G>T , CM000664.2:g.31526137G>T GRCh38
NC_000002.11:g.31751207G>T , CM000664.1:g.31751207G>T GRCh37
NC_000002.10:g.31604711G>T NCBI36
NG_008365.1:g.59835C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.*59C>A MANE Select ENSP00000477587.1:n.*59C>A
ENST00000622030.1:c.*59C>A ENSP00000477587.1:n.*59C>A
NM_000348.3:c.*59C>A NP_000339.2:n.*59C>A
XM_011533069.1:c.*59C>A XP_011531371.1:n.*59C>A
XM_011533070.1:c.*59C>A XP_011531372.1:n.*59C>A
XM_011533071.1:c.*59C>A XP_011531373.1:n.*59C>A
XM_011533072.1:c.*59C>A XP_011531374.1:n.*59C>A
XM_011533069.2:c.*59C>A XP_011531371.1:n.*59C>A
XM_011533072.2:c.*59C>A XP_011531374.1:n.*59C>A
NM_000348.4:c.*59C>A MANE Select NP_000339.2:n.*59C>A
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