Canonical Allele Identifier: CA272672275
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs992036856
gnomAD v3: 15-73329933-A-C
gnomAD v4: 15-73329933-A-C
MyVariant Identifiers: chr15:g.73622274A>C (hg19) chr15:g.73329933A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329933A>C , CM000677.2:g.73329933A>C GRCh38
NC_000015.9:g.73622274A>C , CM000677.1:g.73622274A>C GRCh37
NC_000015.8:g.71409327A>C NCBI36
NG_009063.1:g.44332T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1372-142T>G MANE Select ENSP00000261917.3:n.1372-142T>G
ENST00000261917.3:c.1372-142T>G ENSP00000261917.3:n.1372-142T>G
NM_005477.2:c.1372-142T>G NP_005468.1:n.1372-142T>G
XM_011521148.1:c.154-142T>G XP_011519450.1:n.154-142T>G
XM_011521148.2:c.154-142T>G XP_011519450.1:n.154-142T>G
NM_005477.3:c.1372-142T>G MANE Select NP_005468.1:n.1372-142T>G
Search 100 bp 5'
Search 100 bp 3'