Canonical Allele Identifier: CA105260880

Gene: FGF2

Linked Data

• dbSNP Id: rs1040580104
• MyVariant Identifiers: chr4:g.123772520G>T (hg19) ; chr4:g.122851365G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122851365G>T , CM000666.2:g.122851365G>T	GRCh38
NC_000004.11:g.123772520G>T , CM000666.1:g.123772520G>T	GRCh37
NC_000004.10:g.123991970G>T	NCBI36
NG_029067.1:g.29658G>T
NG_029067.2:g.29658G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264498.9:c.577+24013G>T	ENSP00000264498.4:n.577+24013G>T
ENST00000264498.8:c.577+24013G>T	ENSP00000264498.4:n.577+24013G>T
ENST00000644866.2:c.178+24013G>T MANE Select	ENSP00000494222.1:n.178+24013G>T
ENST00000264498.7:c.577+24013G>T	ENSP00000264498.3:n.577+24013G>T
ENST00000608478.1:c.178+24013G>T	ENSP00000477134.1:n.178+24013G>T
ENST00000614010.4:c.577+24013G>T	ENSP00000478620.1:n.577+24013G>T
NM_002006.4:c.577+24013G>T	NP_001997.5:n.577+24013G>T
NM_001361665.1:c.178+24013G>T	NP_001348594.1:n.178+24013G>T
NM_002006.5:c.577+24013G>T	NP_001997.5:n.577+24013G>T
NM_001361665.2:c.178+24013G>T MANE Select	NP_001348594.1:n.178+24013G>T
NM_002006.6:c.577+24013G>T	NP_001997.5:n.577+24013G>T