Canonical Allele Identifier: CA32667040
Gene: MYOC HGNC NCBI

Linked Data

dbSNP Id: rs962059026
gnomAD v4: 1-171652643-G-A
MyVariant Identifiers: chr1:g.171621783G>A (hg19) chr1:g.171652643G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652643G>A , CM000663.2:g.171652643G>A GRCh38
NC_000001.10:g.171621783G>A , CM000663.1:g.171621783G>A GRCh37
NC_000001.9:g.169888406G>A NCBI36
NG_008859.1:g.4991C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.-32C>T MANE Select ENSP00000037502.5:n.-32C>T
ENST00000037502.10:c.-32C>T ENSP00000037502.5:n.-32C>T
NM_000261.2:c.-32C>T MANE Select NP_000252.1:n.-32C>T
Search 100 bp 5'
Search 100 bp 3'