Canonical Allele Identifier: CA760016744

Gene:

Linked Data

• dbSNP Id: rs1250749388
• gnomAD v3: 2-16458346-G-A
• gnomAD v4: 2-16458346-G-A
• MyVariant Identifiers: chr2:g.16639614G>A (hg19) ; chr2:g.16458346G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.16458346G>A , CM000664.2:g.16458346G>A	GRCh38
NC_000002.11:g.16639614G>A , CM000664.1:g.16639614G>A	GRCh37
NC_000002.10:g.16503095G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_939752.1:n.396-3252C>T