Canonical Allele Identifier: CA350092539
Gene: CRYGD HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.208988878C>T (hg19) chr2:g.208124154C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124154C>T , CM000664.2:g.208124154C>T GRCh38
NC_000002.11:g.208988878C>T , CM000664.1:g.208988878C>T GRCh37
NC_000002.10:g.208697123C>T NCBI36
NG_008039.1:g.5436G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.210G>A MANE Select ENSP00000264376.4:p.Met70Ile
ENST00000264376.4:c.210G>A ENSP00000264376.4:p.Met70Ile
NM_006891.3:c.210G>A NP_008822.2:p.Met70Ile
NR_038437.1:n.97+4929C>T
NM_006891.4:c.210G>A MANE Select NP_008822.2:p.Met70Ile
Search 100 bp 5'
Search 100 bp 3'