Canonical Allele Identifier: CA359707138
Gene: HCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.45645360A>G (hg19) chr5:g.45645258A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645258A>G , CM000667.2:g.45645258A>G GRCh38
NC_000005.9:g.45645360A>G , CM000667.1:g.45645360A>G GRCh37
NC_000005.8:g.45681117A>G NCBI36
NG_042183.1:g.55861T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.776T>C MANE Select ENSP00000307342.4:p.Phe259Ser
ENST00000637256.1:n.4T>C
ENST00000673735.1:c.776T>C ENSP00000501107.1:p.Phe259Ser
ENST00000303230.5:c.776T>C ENSP00000307342.4:p.Phe259Ser
ENST00000634658.1:c.776T>C ENSP00000489134.1:p.Phe259Ser
NM_021072.3:c.776T>C NP_066550.2:p.Phe259Ser
NM_021072.4:c.776T>C MANE Select NP_066550.2:p.Phe259Ser
Search 100 bp 5'
Search 100 bp 3'