Canonical Allele Identifier: CA2063072818
Gene: MYL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110914297T= , CM000674.2:g.110914297T= GRCh38
NC_000012.11:g.111352101T= , CM000674.1:g.111352101T= GRCh37
NC_000012.10:g.109836484T= NCBI36
NG_007554.1:g.11281A= , LRG_393:g.11281A=

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.170-7A= MANE Select ENSP00000228841.8:n.170-7A=
ENST00000663220.1:c.113-7A= ENSP00000499568.1:n.113-7A=
ENST00000228841.12:c.170-7A= ENSP00000228841.7:n.170-7A=
ENST00000548438.1:c.121A= ENSP00000447154.1:p.Thr41=
NM_000432.3:c.170-7A= , LRG_393t1:c.170-7A= NP_000423.2:n.170-7A=
NM_000432.4:c.170-7A= MANE Select NP_000423.2:n.170-7A=
Search 100 bp 5'
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