Canonical Allele Identifier: CA430964581
Gene: CRYGD HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.208988857G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124133G>C , CM000664.2:g.208124133G>C GRCh38
NC_000002.11:g.208988857G>C , CM000664.1:g.208988857G>C GRCh37
NC_000002.10:g.208697102G>C NCBI36
NG_008039.1:g.5457C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.231C>G MANE Select ENSP00000264376.4:p.Arg77=
ENST00000264376.4:c.231C>G ENSP00000264376.4:p.Arg77=
NM_006891.3:c.231C>G NP_008822.2:p.Arg77=
NR_038437.1:n.97+4908G>C
NM_006891.4:c.231C>G MANE Select NP_008822.2:p.Arg77=
Search 100 bp 5'
Search 100 bp 3'