Canonical Allele Identifier: CA2715094344
Gene: HGF HGNC NCBI

Linked Data

dbSNP Id: rs2115806585

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.81711520del , CM000669.2:g.81711520del GRCh38
NC_000007.13:g.81340836del , CM000669.1:g.81340836del GRCh37
NC_000007.12:g.81178772del NCBI36
NG_016274.1:g.63618del
NG_016274.2:g.63618del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222390.11:c.1406del
ENST00000457544.7:c.1391del
ENST00000222390.9:c.1406del
ENST00000457544.6:c.1391del
NM_000601.4:c.1406del
NM_001010932.1:c.1391del
XM_006715956.2:c.1406del
XM_011516115.1:c.1391del
NM_000601.5:c.1406del
NM_001010932.2:c.1391del
XM_011516115.2:c.1391del
NM_000601.6:c.1406del
NM_001010932.3:c.1391del