Canonical Allele Identifier: CA014032
Gene: MYL3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 43128
dbSNP Id: rs145520567

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46858411C>T , CM000665.2:g.46858411C>T GRCh38
NC_000003.11:g.46899901C>T , CM000665.1:g.46899901C>T GRCh37
NC_000003.10:g.46874905C>T NCBI36
NG_007555.2:g.28759G>A , LRG_395:g.28759G>A

Transcript Alleles

HGVS Amino-acid change
NM_000258.2:c.532G>A , LRG_395t1:c.532G>A NP_000249.1:p.Asp178Asn
ENST00000292327.4:c.532G>A ENSP00000292327.4:p.Asp178Asn
ENST00000395869.5:c.532G>A ENSP00000379210.1:p.Asp178Asn