Canonical Allele Identifier: CA386698650
Gene: MYL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.111351996G>C (hg19) chr12:g.110914192G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110914192G>C , CM000674.2:g.110914192G>C GRCh38
NC_000012.11:g.111351996G>C , CM000674.1:g.111351996G>C GRCh37
NC_000012.10:g.109836379G>C NCBI36
NG_007554.1:g.11386C>G , LRG_393:g.11386C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.268C>G MANE Select ENSP00000228841.8:p.Leu90Val
ENST00000663220.1:c.211C>G ENSP00000499568.1:p.Leu71Val
ENST00000228841.12:c.268C>G ENSP00000228841.7:p.Leu90Val
ENST00000548438.1:c.226C>G ENSP00000447154.1:p.Leu76Val
ENST00000549029.1:n.99C>G
NM_000432.3:c.268C>G , LRG_393t1:c.268C>G NP_000423.2:p.Leu90Val
NM_000432.4:c.268C>G MANE Select NP_000423.2:p.Leu90Val
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