Canonical Allele Identifier: CA820839165

Gene:

Linked Data

• dbSNP Id: rs1169598103
• MyVariant Identifiers: chr6:g.151954719del (hg19) ; chr6:g.151633584del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633587del , CM000668.2:g.151633587del	GRCh38
NC_000006.11:g.151954722del , CM000668.1:g.151954722del	GRCh37
NC_000006.10:g.151996415del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3605del