Canonical Allele Identifier: CA2662867496
Gene: CRYGD HGNC NCBI

Linked Data

gnomAD v4: 2-208124023-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124023C>A , CM000664.2:g.208124023C>A GRCh38
NC_000002.11:g.208988747C>A , CM000664.1:g.208988747C>A GRCh37
NC_000002.10:g.208696992C>A NCBI36
NG_008039.1:g.5567G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.252+89G>T MANE Select ENSP00000264376.4:n.252+89G>T
ENST00000264376.4:c.252+89G>T ENSP00000264376.4:n.252+89G>T
NM_006891.3:c.252+89G>T NP_008822.2:n.252+89G>T
NR_038437.1:n.97+4798C>A
NM_006891.4:c.252+89G>T MANE Select NP_008822.2:n.252+89G>T
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