Canonical Allele Identifier: CA1268336144

Linked Data

dbSNP Id: rs546884515

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859710A>T , CM000664.2:g.88859710A>T GRCh38
NC_000002.11:g.89159222A>T , CM000664.1:g.89159222A>T GRCh37
NC_000002.10:g.88940337A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-2027T>A (IGKV1-12) ENSP00000480537.2:n.389-2027T>A
ENST00000430694.5:c.37+1176T>A (IGKC) ENSP00000481923.2:n.37+1176T>A
ENST00000610638.3:c.397+1815T>A (IGKC) ENSP00000484499.3:n.397+1815T>A
ENST00000634828.1:c.382+1815T>A (IGKV1-8) ENSP00000489500.1:n.382+1815T>A