Canonical Allele Identifier: CA342630223
Gene: CHRNB2 HGNC NCBI

Linked Data

gnomAD v4: 1-154571344-G-C
MyVariant Identifiers: chr1:g.154543820G>C (hg19) chr1:g.154571344G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571344G>C , CM000663.2:g.154571344G>C GRCh38
NC_000001.10:g.154543820G>C , CM000663.1:g.154543820G>C GRCh37
NC_000001.9:g.152810444G>C NCBI36
NG_008027.1:g.8564G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.521G>C MANE Select ENSP00000357461.3:p.Arg174Pro
ENST00000636034.1:c.521G>C ENSP00000489703.1:p.Arg174Pro
ENST00000637900.1:c.527G>C ENSP00000490474.1:p.Arg176Pro
ENST00000368476.3:c.521G>C ENSP00000357461.3:p.Arg174Pro
NM_000748.2:c.521G>C NP_000739.1:p.Arg174Pro
XM_017000180.2:c.11G>C XP_016855669.1:p.Arg4Pro
XR_001736952.2:n.773G>C
NM_000748.3:c.521G>C MANE Select NP_000739.1:p.Arg174Pro
Search 100 bp 5'
Search 100 bp 3'