Canonical Allele Identifier: CA350097406
Gene: CRYGC HGNC NCBI

Linked Data

dbSNP Id: rs1574551355
MyVariant Identifiers: chr2:g.208994328A>G (hg19) chr2:g.208129604A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129604A>G , CM000664.2:g.208129604A>G GRCh38
NC_000002.11:g.208994328A>G , CM000664.1:g.208994328A>G GRCh37
NC_000002.10:g.208702573A>G NCBI36
NG_008038.1:g.5227T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.89T>C MANE Select ENSP00000282141.3:p.Phe30Ser
ENST00000282141.3:c.89T>C ENSP00000282141.3:p.Phe30Ser
NM_020989.3:c.89T>C NP_066269.1:p.Phe30Ser
NR_038437.1:n.98-7452A>G
XM_011510661.1:c.89T>C XP_011508963.1:p.Phe30Ser
XM_011510662.1:c.89T>C XP_011508964.1:p.Phe30Ser
XM_011510663.1:c.-41T>C XP_011508965.1:n.-41T>C
NM_020989.4:c.89T>C MANE Select NP_066269.1:p.Phe30Ser
Search 100 bp 5'
Search 100 bp 3'