Canonical Allele Identifier: CA1948159626
Gene:

Linked Data

dbSNP Id: rs1845998079
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444553G>C , CM000673.2:g.2444553G>C GRCh38
NC_000011.9:g.2465783G>C , CM000673.1:g.2465783G>C GRCh37
NC_000011.8:g.2422359G>C NCBI36
NG_008935.1:g.4563G>C , LRG_287:g.4563G>C

Transcript Alleles

HGVS Amino-acid Change
XR_930984.1:n.18C>G
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Search 100 bp 3'