Canonical Allele Identifier: CA1139660825
Community Standard Title: NM_003923.3(FOXH1):c.*21C>A
Gene: FOXH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144474217G>T , CM000670.2:g.144474217G>T GRCh38
NC_000008.10:g.145699600G>T , CM000670.1:g.145699600G>T GRCh37
NC_000008.9:g.145670408G>T NCBI36
NG_030003.1:g.7119C>A

Transcript Alleles

HGVS Amino-acid Change
NM_003923.3:c.*21C>A MANE Select NP_003914.1:n.*21C>A
ENST00000377317.5:c.*21C>A MANE Select ENSP00000366534.4:n.*21C>A
NM_003923.2:c.*21C>A NP_003914.1:n.*21C>A
ENST00000377317.4:c.*21C>A ENSP00000366534.4:n.*21C>A
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