Canonical Allele Identifier: CA2577576344
Gene: MYL3 HGNC NCBI

Linked Data

gnomAD v4: 3-46859402-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46859402T>G , CM000665.2:g.46859402T>G GRCh38
NC_000003.11:g.46900892T>G , CM000665.1:g.46900892T>G GRCh37
NC_000003.10:g.46875896T>G NCBI36
NG_007555.2:g.27768A>C , LRG_395:g.27768A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000431168.2:c.481+73A>C ENSP00000393455.2:n.481+73A>C
ENST00000292327.6:c.481+73A>C MANE Select ENSP00000292327.4:n.481+73A>C
ENST00000653454.1:c.481+73A>C ENSP00000499624.1:n.481+73A>C
ENST00000654597.1:c.481+73A>C ENSP00000499406.1:n.481+73A>C
ENST00000655244.1:n.703+73A>C
ENST00000662933.1:c.481+73A>C ENSP00000499577.1:n.481+73A>C
ENST00000664891.1:n.439+73A>C
ENST00000292327.4:c.481+73A>C ENSP00000292327.4:n.481+73A>C
ENST00000395869.5:c.481+73A>C ENSP00000379210.1:n.481+73A>C
NM_000258.2:c.481+73A>C , LRG_395t1:c.481+73A>C NP_000249.1:n.481+73A>C
NM_000258.3:c.481+73A>C MANE Select NP_000249.1:n.481+73A>C
Search 100 bp 5'
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