Canonical Allele Identifier: CA171602250
Gene: MFHAS1 HGNC NCBI

Linked Data

dbSNP Id: rs893110157
gnomAD v2: 8-8722132-T-A
gnomAD v3: 8-8864622-T-A
gnomAD v4: 8-8864622-T-A
MyVariant Identifiers: chr8:g.8722132T>A (hg19) chr8:g.8864622T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.8864622T>A , CM000670.2:g.8864622T>A GRCh38
NC_000008.10:g.8722132T>A , CM000670.1:g.8722132T>A GRCh37
NC_000008.9:g.8759542T>A NCBI36
NG_009444.1:g.34000A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000276282.7:c.2998+25439A>T MANE Select ENSP00000276282.6:n.2998+25439A>T
ENST00000276282.6:c.2998+25439A>T ENSP00000276282.6:n.2998+25439A>T
NM_004225.2:c.2998+25439A>T NP_004216.2:n.2998+25439A>T
XR_246634.2:n.3534+25439A>T
XM_024447330.1:c.2998+25439A>T XP_024303098.1:n.2998+25439A>T
NM_004225.3:c.2998+25439A>T MANE Select NP_004216.2:n.2998+25439A>T
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