Canonical Allele Identifier: CA539389067
Gene: CRYGD HGNC NCBI

Linked Data

dbSNP Id: rs1476850638
gnomAD v2: 2-208988802-G-A
gnomAD v4: 2-208124078-G-A
MyVariant Identifiers: chr2:g.208988802G>A (hg19) chr2:g.208124078G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124078G>A , CM000664.2:g.208124078G>A GRCh38
NC_000002.11:g.208988802G>A , CM000664.1:g.208988802G>A GRCh37
NC_000002.10:g.208697047G>A NCBI36
NG_008039.1:g.5512C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.252+34C>T MANE Select ENSP00000264376.4:n.252+34C>T
ENST00000264376.4:c.252+34C>T ENSP00000264376.4:n.252+34C>T
NM_006891.3:c.252+34C>T NP_008822.2:n.252+34C>T
NR_038437.1:n.97+4853G>A
NM_006891.4:c.252+34C>T MANE Select NP_008822.2:n.252+34C>T
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