Canonical Allele Identifier: CA393089156
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73616132T>A (hg19) chr15:g.73323791T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323791T>A , CM000677.2:g.73323791T>A GRCh38
NC_000015.9:g.73616132T>A , CM000677.1:g.73616132T>A GRCh37
NC_000015.8:g.71403185T>A NCBI36
NG_009063.1:g.50474A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2302A>T MANE Select ENSP00000261917.3:p.Thr768Ser
ENST00000261917.3:c.2302A>T ENSP00000261917.3:p.Thr768Ser
NM_005477.2:c.2302A>T NP_005468.1:p.Thr768Ser
XM_011521148.1:c.1084A>T XP_011519450.1:p.Thr362Ser
XM_011521148.2:c.1084A>T XP_011519450.1:p.Thr362Ser
NM_005477.3:c.2302A>T MANE Select NP_005468.1:p.Thr768Ser
Search 100 bp 5'
Search 100 bp 3'