Canonical Allele Identifier: CA393097405
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2043134570
gnomAD v3: 15-73367636-C-G
gnomAD v4: 15-73367636-C-G
MyVariant Identifiers: chr15:g.73659977C>G (hg19) chr15:g.73367636C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367636C>G , CM000677.2:g.73367636C>G GRCh38
NC_000015.9:g.73659977C>G , CM000677.1:g.73659977C>G GRCh37
NC_000015.8:g.71447030C>G NCBI36
NG_009063.1:g.6629G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.635G>C MANE Select ENSP00000261917.3:p.Gly212Ala
ENST00000261917.3:c.635G>C ENSP00000261917.3:p.Gly212Ala
NM_005477.2:c.635G>C NP_005468.1:p.Gly212Ala
NM_005477.3:c.635G>C MANE Select NP_005468.1:p.Gly212Ala
Search 100 bp 5'
Search 100 bp 3'