Canonical Allele Identifier: CA73777997

Gene: MYL3

Linked Data

• dbSNP Id: rs182052844
• gnomAD v2: 3-46900891-C-G
• gnomAD v3: 3-46859401-C-G
• gnomAD v4: 3-46859401-C-G
• MyVariant Identifiers: chr3:g.46900891C>G (hg19) ; chr3:g.46859401C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46859401C>G , CM000665.2:g.46859401C>G	GRCh38
NC_000003.11:g.46900891C>G , CM000665.1:g.46900891C>G	GRCh37
NC_000003.10:g.46875895C>G	NCBI36
NG_007555.2:g.27769G>C , LRG_395:g.27769G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000431168.2:c.481+74G>C	ENSP00000393455.2:n.481+74G>C
ENST00000292327.6:c.481+74G>C MANE Select	ENSP00000292327.4:n.481+74G>C
ENST00000653454.1:c.481+74G>C	ENSP00000499624.1:n.481+74G>C
ENST00000654597.1:c.481+74G>C	ENSP00000499406.1:n.481+74G>C
ENST00000655244.1:n.703+74G>C
ENST00000662933.1:c.481+74G>C	ENSP00000499577.1:n.481+74G>C
ENST00000664891.1:n.439+74G>C
ENST00000292327.4:c.481+74G>C	ENSP00000292327.4:n.481+74G>C
ENST00000395869.5:c.481+74G>C	ENSP00000379210.1:n.481+74G>C
NM_000258.2:c.481+74G>C , LRG_395t1:c.481+74G>C	NP_000249.1:n.481+74G>C
NM_000258.3:c.481+74G>C MANE Select	NP_000249.1:n.481+74G>C