Canonical Allele Identifier: CA1215982361

Gene:

Linked Data

• dbSNP Id: rs1665422790
• gnomAD v4: 1-192800670-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192800675del , CM000663.2:g.192800675del	GRCh38
NC_000001.10:g.192769805del , CM000663.1:g.192769805del	GRCh37
NC_000001.9:g.191036428del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429211.2:n.105del