Canonical Allele Identifier: CA393094316
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73332167-G-T
MyVariant Identifiers: chr15:g.73624508G>T (hg19) chr15:g.73332167G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332167G>T , CM000677.2:g.73332167G>T GRCh38
NC_000015.9:g.73624508G>T , CM000677.1:g.73624508G>T GRCh37
NC_000015.8:g.71411561G>T NCBI36
NG_009063.1:g.42098C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1335C>A MANE Select ENSP00000261917.3:p.Phe445Leu
ENST00000261917.3:c.1335C>A ENSP00000261917.3:p.Phe445Leu
NM_005477.2:c.1335C>A NP_005468.1:p.Phe445Leu
XM_011521148.1:c.117C>A XP_011519450.1:p.Phe39Leu
XM_011521148.2:c.117C>A XP_011519450.1:p.Phe39Leu
NM_005477.3:c.1335C>A MANE Select NP_005468.1:p.Phe445Leu
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