Canonical Allele Identifier: CA4316986

Gene: HGF

Linked Data

• dbSNP Id: rs777341007
• ExAC: 7:81355276 A / G
• gnomAD v2: 7-81355276-A-G
• gnomAD v4: 7-81725960-A-G
• MyVariant Identifiers: chr7:g.81355276A>G (hg19) ; chr7:g.81725960A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81725960A>G , CM000669.2:g.81725960A>G	GRCh38
NC_000007.13:g.81355276A>G , CM000669.1:g.81355276A>G	GRCh37
NC_000007.12:g.81193212A>G	NCBI36
NG_016274.1:g.49177T>C
NG_016274.2:g.49177T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000222390.11:c.1098T>C MANE Select	ENSP00000222390.5:p.Phe366=
ENST00000457544.7:c.1083T>C	ENSP00000391238.2:p.Phe361=
ENST00000222390.9:c.1098T>C	ENSP00000222390.5:p.Phe366=
ENST00000457544.6:c.1083T>C	ENSP00000391238.2:p.Phe361=
NM_000601.4:c.1098T>C	NP_000592.3:p.Phe366=
NM_001010932.1:c.1083T>C	NP_001010932.1:p.Phe361=
XM_006715956.2:c.1098T>C	XP_006716019.1:p.Phe366=
XM_011516115.1:c.1083T>C	XP_011514417.1:p.Phe361=
NM_000601.5:c.1098T>C	NP_000592.3:p.Phe366=
NM_001010932.2:c.1083T>C	NP_001010932.1:p.Phe361=
XM_011516115.2:c.1083T>C	XP_011514417.1:p.Phe361=
NM_000601.6:c.1098T>C MANE Select	NP_000592.3:p.Phe366=
NM_001010932.3:c.1083T>C	NP_001010932.1:p.Phe361=