Canonical Allele Identifier: CA1041165999

Gene:

Linked Data

• dbSNP Id: rs2077888512
• gnomAD v3: 2-200033051-T-G
• gnomAD v4: 2-200033051-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.200033051T>G , CM000664.2:g.200033051T>G	GRCh38
NC_000002.11:g.200897774T>G , CM000664.1:g.200897774T>G	GRCh37
NC_000002.10:g.200606019T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923778.1:n.178-22155A>C