Canonical Allele Identifier: CA617508897

Gene:

Linked Data

• dbSNP Id: rs1386413555
• gnomAD v2: 15-38907037-T-G
• gnomAD v3: 15-38614836-T-G
• gnomAD v4: 15-38614836-T-G
• MyVariant Identifiers: chr15:g.38907037T>G (hg19) ; chr15:g.38614836T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38614836T>G , CM000677.2:g.38614836T>G	GRCh38
NC_000015.9:g.38907037T>G , CM000677.1:g.38907037T>G	GRCh37
NC_000015.8:g.36694329T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001751736.1:n.281+2381T>G