Canonical Allele Identifier: CA15489032
Gene: HGF HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.81699165A>T
GRCh37 chr7:g.81328481A>T
gnomAD v2:
7:81328481 A / T
gnomAD v3:
7:81699165 A / T
gnomAD v4:
chr7-81699165-A-T
Joint Max Group AF 0.84720643 (SAS)
Genomes Max Group AF 0.84720643 (SAS)
dbSNP:
1743
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.81699165A>T , CM000669.2:g.81699165A>T GRCh38
NC_000007.13:g.81328481A>T , CM000669.1:g.81328481A>T GRCh37
NC_000007.12:g.81166417A>T NCBI36
NG_016274.2:g.75972T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222390.11:c.*3416T>A MANE Select ENSP00000222390.5:n.*3416T>A
ENST00000222390.9:c.*3416T>A ENSP00000222390.5:n.*3416T>A
XM_006715956.2:c.*3416T>A XP_006716019.1:n.*3416T>A
XM_011516115.1:c.*3416T>A XP_011514417.1:n.*3416T>A
NM_000601.5:c.*3416T>A NP_000592.3:n.*3416T>A
NM_001010932.2:c.*3416T>A NP_001010932.1:n.*3416T>A
NM_000601.6:c.*3416T>A MANE Select NP_000592.3:n.*3416T>A
NM_001010932.3:c.*3416T>A NP_001010932.1:n.*3416T>A
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