Canonical Allele Identifier: CA15108616
Gene: MYOCOS HGNC NCBI

Linked Data

dbSNP Id: rs2421853

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000637303.1:c.234+4221G>A ENSP00000490048.1:n.234+4221G>A