Canonical Allele Identifier: CA367870780

Gene: HGF

Linked Data

• dbSNP Id: rs1180155587
• gnomAD v2: 7-81358951-T-C
• gnomAD v4: 7-81729635-T-C
• MyVariant Identifiers: chr7:g.81358951T>C (hg19) ; chr7:g.81729635T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729635T>C , CM000669.2:g.81729635T>C	GRCh38
NC_000007.13:g.81358951T>C , CM000669.1:g.81358951T>C	GRCh37
NC_000007.12:g.81196887T>C	NCBI36
NG_016274.1:g.45502A>G
NG_016274.2:g.45502A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1010A>G MANE Select	ENSP00000222390.5:p.His337Arg
ENST00000457544.7:c.995A>G	ENSP00000391238.2:p.His332Arg
ENST00000222390.9:c.1010A>G	ENSP00000222390.5:p.His337Arg
ENST00000457544.6:c.995A>G	ENSP00000391238.2:p.His332Arg
NM_000601.4:c.1010A>G	NP_000592.3:p.His337Arg
NM_001010932.1:c.995A>G	NP_001010932.1:p.His332Arg
XM_006715956.2:c.1010A>G	XP_006716019.1:p.His337Arg
XM_011516115.1:c.995A>G	XP_011514417.1:p.His332Arg
NM_000601.5:c.1010A>G	NP_000592.3:p.His337Arg
NM_001010932.2:c.995A>G	NP_001010932.1:p.His332Arg
XM_011516115.2:c.995A>G	XP_011514417.1:p.His332Arg
NM_000601.6:c.1010A>G MANE Select	NP_000592.3:p.His337Arg
NM_001010932.3:c.995A>G	NP_001010932.1:p.His332Arg