Canonical Allele Identifier: CA393095169
Gene: HCN4 HGNC NCBI

Linked Data

COSMIC: COSM5916426
MyVariant Identifiers: chr15:g.73635977C>T (hg19) chr15:g.73343636C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73343636C>T , CM000677.2:g.73343636C>T GRCh38
NC_000015.9:g.73635977C>T , CM000677.1:g.73635977C>T GRCh37
NC_000015.8:g.71423030C>T NCBI36
NG_009063.1:g.30629G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.958G>A MANE Select ENSP00000261917.3:p.Val320Met
ENST00000261917.3:c.958G>A ENSP00000261917.3:p.Val320Met
NM_005477.2:c.958G>A NP_005468.1:p.Val320Met
NM_005477.3:c.958G>A MANE Select NP_005468.1:p.Val320Met
Search 100 bp 5'
Search 100 bp 3'