Canonical Allele Identifier: CA387674373
Gene: FGF9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.22255202T>A (hg19) chr13:g.21681063T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.21681063T>A , CM000675.2:g.21681063T>A GRCh38
NC_000013.10:g.22255202T>A , CM000675.1:g.22255202T>A GRCh37
NC_000013.9:g.21153202T>A NCBI36
NG_016272.1:g.14988T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382353.6:c.299T>A MANE Select ENSP00000371790.5:p.Ile100Lys
ENST00000382353.5:c.299T>A ENSP00000371790.5:p.Ile100Lys
ENST00000461657.1:n.233T>A
NM_002010.2:c.299T>A NP_002001.1:p.Ile100Lys
XM_011534996.1:c.149T>A XP_011533298.1:p.Ile50Lys
XM_011534996.2:c.149T>A XP_011533298.1:p.Ile50Lys
NM_002010.3:c.299T>A MANE Select NP_002001.1:p.Ile100Lys
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