Canonical Allele Identifier: CA352496963
Gene: MYL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46859643T>G , CM000665.2:g.46859643T>G GRCh38
NC_000003.11:g.46901133T>G , CM000665.1:g.46901133T>G GRCh37
NC_000003.10:g.46876137T>G NCBI36
NG_007555.2:g.27527A>C , LRG_395:g.27527A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000431168.2:c.313A>C ENSP00000393455.2:p.Asn105His
ENST00000292327.6:c.313A>C MANE Select ENSP00000292327.4:p.Asn105His
ENST00000653454.1:c.313A>C ENSP00000499624.1:p.Asn105His
ENST00000654597.1:c.313A>C ENSP00000499406.1:p.Asn105His
ENST00000655244.1:n.535A>C
ENST00000662933.1:c.313A>C ENSP00000499577.1:p.Asn105His
ENST00000664891.1:n.271A>C
ENST00000292327.4:c.313A>C ENSP00000292327.4:p.Asn105His
ENST00000395869.5:c.313A>C ENSP00000379210.1:p.Asn105His
NM_000258.2:c.313A>C , LRG_395t1:c.313A>C NP_000249.1:p.Asn105His
NM_000258.3:c.313A>C MANE Select NP_000249.1:p.Asn105His