Canonical Allele Identifier: CA386696735
Gene: MYL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110911104G>C , CM000674.2:g.110911104G>C GRCh38
NC_000012.11:g.111348908G>C , CM000674.1:g.111348908G>C GRCh37
NC_000012.10:g.109833291G>C NCBI36
NG_007554.1:g.14474C>G , LRG_393:g.14474C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.474C>G MANE Select ENSP00000228841.8:p.Ile158Met
ENST00000663220.1:c.417C>G ENSP00000499568.1:p.Ile139Met
ENST00000228841.12:c.474C>G ENSP00000228841.7:p.Ile158Met
ENST00000548438.1:c.432C>G ENSP00000447154.1:p.Ile144Met
NM_000432.3:c.474C>G , LRG_393t1:c.474C>G NP_000423.2:p.Ile158Met
NM_000432.4:c.474C>G MANE Select NP_000423.2:p.Ile158Met