Canonical Allele Identifier: CA367869995

Gene: HGF

Linked Data

• dbSNP Id: rs1321819869
• MyVariant Identifiers: chr7:g.81355274G>A (hg19) ; chr7:g.81725958G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81725958G>A , CM000669.2:g.81725958G>A	GRCh38
NC_000007.13:g.81355274G>A , CM000669.1:g.81355274G>A	GRCh37
NC_000007.12:g.81193210G>A	NCBI36
NG_016274.1:g.49179C>T
NG_016274.2:g.49179C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1100C>T MANE Select	ENSP00000222390.5:p.Thr367Ile
ENST00000457544.7:c.1085C>T	ENSP00000391238.2:p.Thr362Ile
ENST00000222390.9:c.1100C>T	ENSP00000222390.5:p.Thr367Ile
ENST00000457544.6:c.1085C>T	ENSP00000391238.2:p.Thr362Ile
NM_000601.4:c.1100C>T	NP_000592.3:p.Thr367Ile
NM_001010932.1:c.1085C>T	NP_001010932.1:p.Thr362Ile
XM_006715956.2:c.1100C>T	XP_006716019.1:p.Thr367Ile
XM_011516115.1:c.1085C>T	XP_011514417.1:p.Thr362Ile
NM_000601.5:c.1100C>T	NP_000592.3:p.Thr367Ile
NM_001010932.2:c.1085C>T	NP_001010932.1:p.Thr362Ile
XM_011516115.2:c.1085C>T	XP_011514417.1:p.Thr362Ile
NM_000601.6:c.1100C>T MANE Select	NP_000592.3:p.Thr367Ile
NM_001010932.3:c.1085C>T	NP_001010932.1:p.Thr362Ile