Canonical Allele Identifier: CA393098435
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73367969-G-C
MyVariant Identifiers: chr15:g.73660310G>C (hg19) chr15:g.73367969G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367969G>C , CM000677.2:g.73367969G>C GRCh38
NC_000015.9:g.73660310G>C , CM000677.1:g.73660310G>C GRCh37
NC_000015.8:g.71447363G>C NCBI36
NG_009063.1:g.6296C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.302C>G MANE Select ENSP00000261917.3:p.Ala101Gly
ENST00000261917.3:c.302C>G ENSP00000261917.3:p.Ala101Gly
NM_005477.2:c.302C>G NP_005468.1:p.Ala101Gly
NM_005477.3:c.302C>G MANE Select NP_005468.1:p.Ala101Gly
Search 100 bp 5'
Search 100 bp 3'