Canonical Allele Identifier: CA12635032
Gene: HGF HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.81720907G>A
GRCh37 chr7:g.81350223G>A
gnomAD v2:
7:81350223 G / A
gnomAD v3:
7:81720907 G / A
gnomAD v4:
chr7-81720907-G-A
Joint Max Group AF 0.94866936 (AFR)
Genomes Max Group AF 0.94684065 (AFR)
Exomes Max Group AF 0.9446609 (AFR)
ClinVar RCV:
RCV001645309
ClinVar Variation:
1241564
dbSNP:
10272030
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.81720907G>A , CM000669.2:g.81720907G>A GRCh38
NC_000007.13:g.81350223G>A , CM000669.1:g.81350223G>A GRCh37
NC_000007.12:g.81188159G>A NCBI36
NG_016274.1:g.54230C>T
NG_016274.2:g.54230C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222390.11:c.1169-60C>T MANE Select ENSP00000222390.5:n.1169-60C>T
ENST00000457544.7:c.1154-60C>T ENSP00000391238.2:n.1154-60C>T
ENST00000222390.9:c.1169-60C>T ENSP00000222390.5:n.1169-60C>T
ENST00000457544.6:c.1154-60C>T ENSP00000391238.2:n.1154-60C>T
NM_000601.4:c.1169-60C>T NP_000592.3:n.1169-60C>T
NM_001010932.1:c.1154-60C>T NP_001010932.1:n.1154-60C>T
XM_006715956.2:c.1169-60C>T XP_006716019.1:n.1169-60C>T
XM_011516115.1:c.1154-60C>T XP_011514417.1:n.1154-60C>T
NM_000601.5:c.1169-60C>T NP_000592.3:n.1169-60C>T
NM_001010932.2:c.1154-60C>T NP_001010932.1:n.1154-60C>T
XM_011516115.2:c.1154-60C>T XP_011514417.1:n.1154-60C>T
NM_000601.6:c.1169-60C>T MANE Select NP_000592.3:n.1169-60C>T
NM_001010932.3:c.1154-60C>T NP_001010932.1:n.1154-60C>T
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