Canonical Allele Identifier: CA763924280
Gene: CRYGD HGNC NCBI

Linked Data

dbSNP Id: rs1444979739
gnomAD v3: 2-208124040-T-G
gnomAD v4: 2-208124040-T-G
MyVariant Identifiers: chr2:g.208988764T>G (hg19) chr2:g.208124040T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124040T>G , CM000664.2:g.208124040T>G GRCh38
NC_000002.11:g.208988764T>G , CM000664.1:g.208988764T>G GRCh37
NC_000002.10:g.208697009T>G NCBI36
NG_008039.1:g.5550A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.252+72A>C MANE Select ENSP00000264376.4:n.252+72A>C
ENST00000264376.4:c.252+72A>C ENSP00000264376.4:n.252+72A>C
NM_006891.3:c.252+72A>C NP_008822.2:n.252+72A>C
NR_038437.1:n.97+4815T>G
NM_006891.4:c.252+72A>C MANE Select NP_008822.2:n.252+72A>C
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