Canonical Allele Identifier: CA1139934777
Gene: MYOCOS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171630813G= , CM000663.2:g.171630813G= GRCh38
NC_000001.10:g.171599953G= , CM000663.1:g.171599953G= GRCh37
NC_000001.9:g.169866576G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637303.1:c.234+4221G= ENSP00000490048.1:n.234+4221G=