Canonical Allele Identifier: CA811000300
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1375617422
gnomAD v3: 5-44365368-A-G
gnomAD v4: 5-44365368-A-G
MyVariant Identifiers: chr5:g.44365470A>G (hg19) chr5:g.44365368A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365368A>G , CM000667.2:g.44365368A>G GRCh38
NC_000005.9:g.44365470A>G , CM000667.1:g.44365470A>G GRCh37
NC_000005.8:g.44401227A>G NCBI36
NG_011446.1:g.28315T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.325+22990T>C MANE Select ENSP00000264664.4:n.325+22990T>C
ENST00000264664.4:c.325+22990T>C ENSP00000264664.4:n.325+22990T>C
NM_004465.1:c.325+22990T>C NP_004456.1:n.325+22990T>C
XM_005248264.2:c.325+22990T>C XP_005248321.1:n.325+22990T>C
XM_005248264.4:c.325+22990T>C XP_005248321.1:n.325+22990T>C
NM_004465.2:c.325+22990T>C MANE Select NP_004456.1:n.325+22990T>C
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