Canonical Allele Identifier: CA4317012

Gene: HGF

Linked Data

• ClinVar Variation Id: 1905776
• ClinVar RCV Id: RCV002583757
• dbSNP Id: rs757186641
• ExAC: 7:81358956 G / A
• gnomAD v2: 7-81358956-G-A
• gnomAD v3: 7-81729640-G-A
• gnomAD v4: 7-81729640-G-A
• MyVariant Identifiers: chr7:g.81358956G>A (hg19) ; chr7:g.81729640G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729640G>A , CM000669.2:g.81729640G>A	GRCh38
NC_000007.13:g.81358956G>A , CM000669.1:g.81358956G>A	GRCh37
NC_000007.12:g.81196892G>A	NCBI36
NG_016274.1:g.45497C>T
NG_016274.2:g.45497C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1005C>T MANE Select	ENSP00000222390.5:p.His335=
ENST00000457544.7:c.990C>T	ENSP00000391238.2:p.His330=
ENST00000222390.9:c.1005C>T	ENSP00000222390.5:p.His335=
ENST00000457544.6:c.990C>T	ENSP00000391238.2:p.His330=
NM_000601.4:c.1005C>T	NP_000592.3:p.His335=
NM_001010932.1:c.990C>T	NP_001010932.1:p.His330=
XM_006715956.2:c.1005C>T	XP_006716019.1:p.His335=
XM_011516115.1:c.990C>T	XP_011514417.1:p.His330=
NM_000601.5:c.1005C>T	NP_000592.3:p.His335=
NM_001010932.2:c.990C>T	NP_001010932.1:p.His330=
XM_011516115.2:c.990C>T	XP_011514417.1:p.His330=
NM_000601.6:c.1005C>T MANE Select	NP_000592.3:p.His335=
NM_001010932.3:c.990C>T	NP_001010932.1:p.His330=