Canonical Allele Identifier: CA2727312925
Gene: MYL2 HGNC NCBI

Linked Data

dbSNP Id: rs2136767347

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110911004_110911005insGTGTT , CM000674.2:g.110911004_110911005insGTGTT GRCh38
NC_000012.11:g.111348808_111348809insGTGTT , CM000674.1:g.111348808_111348809insGTGTT GRCh37
NC_000012.10:g.109833191_109833192insGTGTT NCBI36
NG_007554.1:g.14574_14575insACACA , LRG_393:g.14574_14575insACACA

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.*73_*74insACACA MANE Select ENSP00000228841.8:n.*73_*74insACACA
ENST00000663220.1:c.*73_*74insACACA ENSP00000499568.1:n.*73_*74insACACA
ENST00000228841.12:c.*73_*74insACACA ENSP00000228841.7:n.*73_*74insACACA
ENST00000548438.1:c.*73_*74insACACA ENSP00000447154.1:n.*73_*74insACACA
NM_000432.3:c.*73_*74insACACA , LRG_393t1:c.*73_*74insACACA NP_000423.2:n.*73_*74insACACA
NM_000432.4:c.*73_*74insACACA MANE Select NP_000423.2:n.*73_*74insACACA