Canonical Allele Identifier: CA456129147

Gene: HGF

Linked Data

• dbSNP Id: rs1471790055
• gnomAD v2: 7-81358950-A-G
• gnomAD v4: 7-81729634-A-G
• MyVariant Identifiers: chr7:g.81358950A>G (hg19) ; chr7:g.81729634A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729634A>G , CM000669.2:g.81729634A>G	GRCh38
NC_000007.13:g.81358950A>G , CM000669.1:g.81358950A>G	GRCh37
NC_000007.12:g.81196886A>G	NCBI36
NG_016274.1:g.45503T>C
NG_016274.2:g.45503T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1011T>C MANE Select	ENSP00000222390.5:p.His337=
ENST00000457544.7:c.996T>C	ENSP00000391238.2:p.His332=
ENST00000222390.9:c.1011T>C	ENSP00000222390.5:p.His337=
ENST00000457544.6:c.996T>C	ENSP00000391238.2:p.His332=
NM_000601.4:c.1011T>C	NP_000592.3:p.His337=
NM_001010932.1:c.996T>C	NP_001010932.1:p.His332=
XM_006715956.2:c.1011T>C	XP_006716019.1:p.His337=
XM_011516115.1:c.996T>C	XP_011514417.1:p.His332=
NM_000601.5:c.1011T>C	NP_000592.3:p.His337=
NM_001010932.2:c.996T>C	NP_001010932.1:p.His332=
XM_011516115.2:c.996T>C	XP_011514417.1:p.His332=
NM_000601.6:c.1011T>C MANE Select	NP_000592.3:p.His337=
NM_001010932.3:c.996T>C	NP_001010932.1:p.His332=