Canonical Allele Identifier: CA531729669

Gene: SRD5A2

Linked Data

• dbSNP Id: rs1462485173
• gnomAD v2: 2-31811873-A-G
• gnomAD v3: 2-31586804-A-G
• gnomAD v4: 2-31586804-A-G
• MyVariant Identifiers: chr2:g.31811873A>G (hg19) ; chr2:g.31586804A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31586804A>G , CM000664.2:g.31586804A>G	GRCh38
NC_000002.11:g.31811873A>G , CM000664.1:g.31811873A>G	GRCh37
NC_000002.10:g.31665377A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011533070.1:c.27-53038T>C	XP_011531372.1:n.27-53038T>C
XM_011533071.1:c.27-53038T>C	XP_011531373.1:n.27-53038T>C
XM_011533072.1:c.27-53038T>C	XP_011531374.1:n.27-53038T>C
XM_011533072.2:c.27-53038T>C	XP_011531374.1:n.27-53038T>C