Canonical Allele Identifier: CA425627286
Gene: SRD5A2 HGNC NCBI

Linked Data

gnomAD v4: 2-31580906-C-T
MyVariant Identifiers: chr2:g.31805975C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31580906C>T , CM000664.2:g.31580906C>T GRCh38
NC_000002.11:g.31805975C>T , CM000664.1:g.31805975C>T GRCh37
NC_000002.10:g.31659479C>T NCBI36
NG_008365.1:g.5066G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.-6G>A MANE Select ENSP00000477587.1:n.-6G>A
ENST00000622030.1:c.-6G>A ENSP00000477587.1:n.-6G>A
NM_000348.3:c.-6G>A NP_000339.2:n.-6G>A
XM_011533068.1:c.-6G>A XP_011531370.1:n.-6G>A
XM_011533070.1:c.27-47140G>A XP_011531372.1:n.27-47140G>A
XM_011533071.1:c.27-47140G>A XP_011531373.1:n.27-47140G>A
XM_011533072.1:c.27-47140G>A XP_011531374.1:n.27-47140G>A
XM_011533072.2:c.27-47140G>A XP_011531374.1:n.27-47140G>A
NM_000348.4:c.-6G>A MANE Select NP_000339.2:n.-6G>A
Search 100 bp 5'
Search 100 bp 3'