Canonical Allele Identifier: CA2063073019
Gene: MYL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110914390C= , CM000674.2:g.110914390C= GRCh38
NC_000012.11:g.111352194C= , CM000674.1:g.111352194C= GRCh37
NC_000012.10:g.109836577C= NCBI36
NG_007554.1:g.11188G= , LRG_393:g.11188G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000228841.15:c.170-100G= MANE Select ENSP00000228841.8:n.170-100G=
ENST00000663220.1:c.113-100G= ENSP00000499568.1:n.113-100G=
ENST00000228841.12:c.170-100G= ENSP00000228841.7:n.170-100G=
ENST00000548438.1:c.94-66G= ENSP00000447154.1:n.94-66G=
NM_000432.3:c.170-100G= , LRG_393t1:c.170-100G= NP_000423.2:n.170-100G=
NM_000432.4:c.170-100G= MANE Select NP_000423.2:n.170-100G=
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