Canonical Allele Identifier: CA768889912
Gene:

Linked Data

dbSNP Id: rs1359623858
gnomAD v3: 2-41534497-T-C
gnomAD v4: 2-41534497-T-C
MyVariant Identifiers: chr2:g.41761637T>C (hg19) chr2:g.41534497T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534497T>C , CM000664.2:g.41534497T>C GRCh38
NC_000002.11:g.41761637T>C , CM000664.1:g.41761637T>C GRCh37
NC_000002.10:g.41615141T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939996.1:n.181+3229A>G
XR_939997.1:n.146+3229A>G
XR_939997.2:n.9529+3229A>G
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