Canonical Allele Identifier: CA571557179

Gene:

Linked Data

• dbSNP Id: rs1419099185
• gnomAD v2: 6-161089819-GGTA-G
• gnomAD v3: 6-160668787-GGTA-G
• gnomAD v4: 6-160668787-GGTA-G
• MyVariant Identifiers: chr6:g.161089820_161089822del (hg19) ; chr6:g.160668788_160668790del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160668788_160668790del , CM000668.2:g.160668788_160668790del	GRCh38
NC_000006.11:g.161089820_161089822del , CM000668.1:g.161089820_161089822del	GRCh37
NC_000006.10:g.161009810_161009812del	NCBI36
NG_016147.1:g.2586_2588del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452651.1:n.115-2417_115-2415del