Canonical Allele Identifier: CA420670474
Gene: SF3B4 HGNC NCBI

Linked Data

gnomAD v4: 1-149923638-G-T
MyVariant Identifiers: chr1:g.149895530G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149923638G>T , CM000663.2:g.149923638G>T GRCh38
NC_000001.10:g.149895530G>T , CM000663.1:g.149895530G>T GRCh37
NC_000001.9:g.148162154G>T NCBI36
NG_032777.1:g.9615C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000271628.9:c.1179C>A MANE Select ENSP00000271628.8:p.Pro393=
ENST00000271628.8:c.1179C>A ENSP00000271628.8:p.Pro393=
NM_005850.4:c.1179C>A NP_005841.1:p.Pro393=
NM_005850.5:c.1179C>A MANE Select NP_005841.1:p.Pro393=
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Search 100 bp 3'