Canonical Allele Identifier: CA2665478447

Gene: MYL3

Linked Data

• gnomAD v4: 3-46859446-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46859446G>A , CM000665.2:g.46859446G>A	GRCh38
NC_000003.11:g.46900936G>A , CM000665.1:g.46900936G>A	GRCh37
NC_000003.10:g.46875940G>A	NCBI36
NG_007555.2:g.27724C>T , LRG_395:g.27724C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000431168.2:c.481+29C>T	ENSP00000393455.2:n.481+29C>T
ENST00000292327.6:c.481+29C>T MANE Select	ENSP00000292327.4:n.481+29C>T
ENST00000653454.1:c.481+29C>T	ENSP00000499624.1:n.481+29C>T
ENST00000654597.1:c.481+29C>T	ENSP00000499406.1:n.481+29C>T
ENST00000655244.1:n.703+29C>T
ENST00000662933.1:c.481+29C>T	ENSP00000499577.1:n.481+29C>T
ENST00000664891.1:n.439+29C>T
ENST00000292327.4:c.481+29C>T	ENSP00000292327.4:n.481+29C>T
ENST00000395869.5:c.481+29C>T	ENSP00000379210.1:n.481+29C>T
NM_000258.2:c.481+29C>T , LRG_395t1:c.481+29C>T	NP_000249.1:n.481+29C>T
NM_000258.3:c.481+29C>T MANE Select	NP_000249.1:n.481+29C>T