Canonical Allele Identifier: CA352093
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 222737
ClinVar RCV Id: RCV000208495 RCV000426551 RCV000817802
dbSNP Id: rs869025486
MyVariant Identifiers: chr3:g.46900995C>T (hg19) chr3:g.46859505C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46859505C>T , CM000665.2:g.46859505C>T GRCh38
NC_000003.11:g.46900995C>T , CM000665.1:g.46900995C>T GRCh37
NC_000003.10:g.46875999C>T NCBI36
NG_007555.2:g.27665G>A , LRG_395:g.27665G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000431168.2:c.451G>A ENSP00000393455.2:p.Ala151Thr
ENST00000292327.6:c.451G>A MANE Select ENSP00000292327.4:p.Ala151Thr
ENST00000653454.1:c.451G>A ENSP00000499624.1:p.Ala151Thr
ENST00000654597.1:c.451G>A ENSP00000499406.1:p.Ala151Thr
ENST00000655244.1:n.673G>A
ENST00000662933.1:c.451G>A ENSP00000499577.1:p.Ala151Thr
ENST00000664891.1:n.409G>A
ENST00000292327.4:c.451G>A ENSP00000292327.4:p.Ala151Thr
ENST00000395869.5:c.451G>A ENSP00000379210.1:p.Ala151Thr
NM_000258.2:c.451G>A , LRG_395t1:c.451G>A NP_000249.1:p.Ala151Thr
NM_000258.3:c.451G>A MANE Select NP_000249.1:p.Ala151Thr
Search 100 bp 5'
Search 100 bp 3'