Canonical Allele Identifier: CA4316899

Gene: HGF

Linked Data

• dbSNP Id: rs763164743
• ExAC: 7:81340759 G / C
• gnomAD v2: 7-81340759-G-C
• gnomAD v4: 7-81711443-G-C
• MyVariant Identifiers: chr7:g.81340759G>C (hg19) ; chr7:g.81711443G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81711443G>C , CM000669.2:g.81711443G>C	GRCh38
NC_000007.13:g.81340759G>C , CM000669.1:g.81340759G>C	GRCh37
NC_000007.12:g.81178695G>C	NCBI36
NG_016274.1:g.63694C>G
NG_016274.2:g.63694C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1444+38C>G MANE Select	ENSP00000222390.5:n.1444+38C>G
ENST00000457544.7:c.1429+38C>G	ENSP00000391238.2:n.1429+38C>G
ENST00000222390.9:c.1444+38C>G	ENSP00000222390.5:n.1444+38C>G
ENST00000457544.6:c.1429+38C>G	ENSP00000391238.2:n.1429+38C>G
NM_000601.4:c.1444+38C>G	NP_000592.3:n.1444+38C>G
NM_001010932.1:c.1429+38C>G	NP_001010932.1:n.1429+38C>G
XM_006715956.2:c.1444+38C>G	XP_006716019.1:n.1444+38C>G
XM_011516115.1:c.1429+38C>G	XP_011514417.1:n.1429+38C>G
NM_000601.5:c.1444+38C>G	NP_000592.3:n.1444+38C>G
NM_001010932.2:c.1429+38C>G	NP_001010932.1:n.1429+38C>G
XM_011516115.2:c.1429+38C>G	XP_011514417.1:n.1429+38C>G
NM_000601.6:c.1444+38C>G MANE Select	NP_000592.3:n.1444+38C>G
NM_001010932.3:c.1429+38C>G	NP_001010932.1:n.1429+38C>G