Canonical Allele Identifier: CA555654971
Gene:

Linked Data

dbSNP Id: rs1241406659
gnomAD v2: 4-149570713-C-T
gnomAD v3: 4-148649561-C-T
gnomAD v4: 4-148649561-C-T
MyVariant Identifiers: chr4:g.149570713C>T (hg19) chr4:g.148649561C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148649561C>T , CM000666.2:g.148649561C>T GRCh38
NC_000004.11:g.149570713C>T , CM000666.1:g.149570713C>T GRCh37
NC_000004.10:g.149790163C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939336.1:n.437-30693G>A
XR_001741441.1:n.1745+104977C>T
XR_939336.3:n.2921-30693G>A
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