Canonical Allele Identifier: CA393088203
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1370321950
gnomAD v2: 15-73615691-C-G
gnomAD v4: 15-73323350-C-G
MyVariant Identifiers: chr15:g.73615691C>G (hg19) chr15:g.73323350C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323350C>G , CM000677.2:g.73323350C>G GRCh38
NC_000015.9:g.73615691C>G , CM000677.1:g.73615691C>G GRCh37
NC_000015.8:g.71402744C>G NCBI36
NG_009063.1:g.50915G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2743G>C MANE Select ENSP00000261917.3:p.Gly915Arg
ENST00000261917.3:c.2743G>C ENSP00000261917.3:p.Gly915Arg
NM_005477.2:c.2743G>C NP_005468.1:p.Gly915Arg
XM_011521148.1:c.1525G>C XP_011519450.1:p.Gly509Arg
XM_011521148.2:c.1525G>C XP_011519450.1:p.Gly509Arg
NM_005477.3:c.2743G>C MANE Select NP_005468.1:p.Gly915Arg
Search 100 bp 5'
Search 100 bp 3'