Canonical Allele Identifier: CA433474543
Gene: MYL3 HGNC NCBI

Linked Data

dbSNP Id: rs1575498192
MyVariant Identifiers: chr3:g.46902209T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46860719T>G , CM000665.2:g.46860719T>G GRCh38
NC_000003.11:g.46902209T>G , CM000665.1:g.46902209T>G GRCh37
NC_000003.10:g.46877213T>G NCBI36
NG_007555.2:g.26451A>C , LRG_395:g.26451A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000431168.2:c.264A>C ENSP00000393455.2:p.Thr88=
ENST00000292327.6:c.264A>C MANE Select ENSP00000292327.4:p.Thr88=
ENST00000653454.1:c.264A>C ENSP00000499624.1:p.Thr88=
ENST00000654597.1:c.264A>C ENSP00000499406.1:p.Thr88=
ENST00000655244.1:n.486A>C
ENST00000662933.1:c.264A>C ENSP00000499577.1:p.Thr88=
ENST00000664891.1:n.222A>C
ENST00000292327.4:c.264A>C ENSP00000292327.4:p.Thr88=
ENST00000395869.5:c.264A>C ENSP00000379210.1:p.Thr88=
NM_000258.2:c.264A>C , LRG_395t1:c.264A>C NP_000249.1:p.Thr88=
NM_000258.3:c.264A>C MANE Select NP_000249.1:p.Thr88=
Search 100 bp 5'
Search 100 bp 3'