Canonical Allele Identifier: CA161089691

Gene: HGF

Linked Data

• dbSNP Id: rs1016906881
• gnomAD v2: 7-81358965-C-T
• gnomAD v3: 7-81729649-C-T
• gnomAD v4: 7-81729649-C-T
• MyVariant Identifiers: chr7:g.81358965C>T (hg19) ; chr7:g.81729649C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729649C>T , CM000669.2:g.81729649C>T	GRCh38
NC_000007.13:g.81358965C>T , CM000669.1:g.81358965C>T	GRCh37
NC_000007.12:g.81196901C>T	NCBI36
NG_016274.1:g.45488G>A
NG_016274.2:g.45488G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000222390.11:c.996G>A MANE Select	ENSP00000222390.5:p.Gln332=
ENST00000457544.7:c.981G>A	ENSP00000391238.2:p.Gln327=
ENST00000222390.9:c.996G>A	ENSP00000222390.5:p.Gln332=
ENST00000457544.6:c.981G>A	ENSP00000391238.2:p.Gln327=
NM_000601.4:c.996G>A	NP_000592.3:p.Gln332=
NM_001010932.1:c.981G>A	NP_001010932.1:p.Gln327=
XM_006715956.2:c.996G>A	XP_006716019.1:p.Gln332=
XM_011516115.1:c.981G>A	XP_011514417.1:p.Gln327=
NM_000601.5:c.996G>A	NP_000592.3:p.Gln332=
NM_001010932.2:c.981G>A	NP_001010932.1:p.Gln327=
XM_011516115.2:c.981G>A	XP_011514417.1:p.Gln327=
NM_000601.6:c.996G>A MANE Select	NP_000592.3:p.Gln332=
NM_001010932.3:c.981G>A	NP_001010932.1:p.Gln327=