Canonical Allele Identifier: CA342273439
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs2092568961
MyVariant Identifiers: chr1:g.149895534G>A (hg19) chr1:g.149923642G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149923642G>A , CM000663.2:g.149923642G>A GRCh38
NC_000001.10:g.149895534G>A , CM000663.1:g.149895534G>A GRCh37
NC_000001.9:g.148162158G>A NCBI36
NG_032777.1:g.9611C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000271628.9:c.1175C>T MANE Select ENSP00000271628.8:p.Pro392Leu
ENST00000271628.8:c.1175C>T ENSP00000271628.8:p.Pro392Leu
NM_005850.4:c.1175C>T NP_005841.1:p.Pro392Leu
NM_005850.5:c.1175C>T MANE Select NP_005841.1:p.Pro392Leu
Search 100 bp 5'
Search 100 bp 3'