Canonical Allele Identifier: CA539388999
Gene: CRYGC HGNC NCBI

Linked Data

dbSNP Id: rs1204463382
gnomAD v2: 2-208994567-C-A
gnomAD v3: 2-208129843-C-A
gnomAD v4: 2-208129843-C-A
MyVariant Identifiers: chr2:g.208994567C>A (hg19) chr2:g.208129843C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129843C>A , CM000664.2:g.208129843C>A GRCh38
NC_000002.11:g.208994567C>A , CM000664.1:g.208994567C>A GRCh37
NC_000002.10:g.208702812C>A NCBI36
NG_008038.1:g.4988G>T

Transcript Alleles

HGVS Amino-acid Change
NR_038437.1:n.98-7213C>A
XM_011510661.1:c.-51G>T XP_011508963.1:n.-51G>T
XM_011510662.1:c.-51G>T XP_011508964.1:n.-51G>T
XM_011510663.1:c.-120-160G>T XP_011508965.1:n.-120-160G>T
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