Canonical Allele Identifier: CA842880545
Gene: HGF HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.81701064C>A
GRCh37 chr7:g.81330380C>A
gnomAD v3:
7:81701064 C / A
gnomAD v4:
chr7-81701064-C-A
Joint Max Group AF 0.00000491 (NFE)
Genomes Max Group AF 0.00000491 (NFE)
dbSNP:
4732402
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.81701064C>A , CM000669.2:g.81701064C>A GRCh38
NC_000007.13:g.81330380C>A , CM000669.1:g.81330380C>A GRCh37
NC_000007.12:g.81168316C>A NCBI36
NG_016274.1:g.74073G>T
NG_016274.2:g.74073G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222390.11:c.*1517G>T MANE Select ENSP00000222390.5:n.*1517G>T
ENST00000222390.9:c.*1517G>T ENSP00000222390.5:n.*1517G>T
XM_006715956.2:c.*1517G>T XP_006716019.1:n.*1517G>T
XM_011516115.1:c.*1517G>T XP_011514417.1:n.*1517G>T
NM_000601.5:c.*1517G>T NP_000592.3:n.*1517G>T
NM_001010932.2:c.*1517G>T NP_001010932.1:n.*1517G>T
XM_011516115.2:c.*1517G>T XP_011514417.1:n.*1517G>T
NM_000601.6:c.*1517G>T MANE Select NP_000592.3:n.*1517G>T
NM_001010932.3:c.*1517G>T NP_001010932.1:n.*1517G>T
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