Canonical Allele Identifier: CA93117934

Gene:

Linked Data

• dbSNP Id: rs781718607
• MyVariant Identifiers: chr4:g.12579985_12579988del (hg19) ; chr4:g.12578361_12578364del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.12578364_12578367del , CM000666.2:g.12578364_12578367del	GRCh38
NC_000004.11:g.12579988_12579991del , CM000666.1:g.12579988_12579991del	GRCh37
NC_000004.10:g.12189086_12189089del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_925406.1:n.106+30978_106+30981del
XR_001741374.1:n.254+44291_254+44294del
XR_925406.3:n.140+30978_140+30981del