Canonical Allele Identifier: CA171602283
Gene: MFHAS1 HGNC NCBI

Linked Data

dbSNP Id: rs193233977
MyVariant Identifiers: chr8:g.8722282C>T (hg19) chr8:g.8864772C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.8864772C>T , CM000670.2:g.8864772C>T GRCh38
NC_000008.10:g.8722282C>T , CM000670.1:g.8722282C>T GRCh37
NC_000008.9:g.8759692C>T NCBI36
NG_009444.1:g.33850G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000276282.7:c.2998+25289G>A MANE Select ENSP00000276282.6:n.2998+25289G>A
ENST00000276282.6:c.2998+25289G>A ENSP00000276282.6:n.2998+25289G>A
NM_004225.2:c.2998+25289G>A NP_004216.2:n.2998+25289G>A
XR_246634.2:n.3534+25289G>A
XM_024447330.1:c.2998+25289G>A XP_024303098.1:n.2998+25289G>A
NM_004225.3:c.2998+25289G>A MANE Select NP_004216.2:n.2998+25289G>A
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