Canonical Allele Identifier: CA212938832
Gene: HIF1AN HGNC NCBI

Linked Data

dbSNP Id: rs1030787459
MyVariant Identifiers: chr10:g.102302494C>A (hg19) chr10:g.100542737C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100542737C>A , CM000672.2:g.100542737C>A GRCh38
NC_000010.10:g.102302494C>A , CM000672.1:g.102302494C>A GRCh37
NC_000010.9:g.102292484C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000299163.7:c.577+1955C>A MANE Select ENSP00000299163.4:n.577+1955C>A
ENST00000299163.6:c.577+1955C>A ENSP00000299163.4:n.577+1955C>A
ENST00000478787.1:n.341+1955C>A
ENST00000526476.5:c.*384+1955C>A ENSP00000432791.1:n.*384+1955C>A
ENST00000533589.6:c.256+1955C>A ENSP00000433360.2:n.256+1955C>A
NM_017902.2:c.577+1955C>A NP_060372.2:n.577+1955C>A
XM_011539940.1:c.637+1955C>A XP_011538242.1:n.637+1955C>A
XM_011539941.1:c.256+1955C>A XP_011538243.1:n.256+1955C>A
XM_011539940.2:c.637+1955C>A XP_011538242.1:n.637+1955C>A
NM_017902.3:c.577+1955C>A MANE Select NP_060372.2:n.577+1955C>A
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