Canonical Allele Identifier: CA605243855
Gene: MYG1 HGNC NCBI

Linked Data

dbSNP Id: rs1420443662
gnomAD v2: 12-53700964-C-A
gnomAD v4: 12-53307180-C-A
MyVariant Identifiers: chr12:g.53700964C>A (hg19) chr12:g.53307180C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53307180C>A , CM000674.2:g.53307180C>A GRCh38
NC_000012.11:g.53700964C>A , CM000674.1:g.53700964C>A GRCh37
NC_000012.10:g.51987231C>A NCBI36
NG_016775.1:g.19449G>T

Transcript Alleles

HGVS Amino-acid Change
NM_021640.3:c.*31C>A NP_067653.3:n.*31C>A
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