Canonical Allele Identifier: CA130192036
Gene: ADAM19 HGNC NCBI

Linked Data

dbSNP Id: rs76808472
MyVariant Identifiers: chr5:g.156995961C>T (hg19) chr5:g.157568953C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157568953C>T , CM000667.2:g.157568953C>T GRCh38
NC_000005.9:g.156995961C>T , CM000667.1:g.156995961C>T GRCh37
NC_000005.8:g.156928539C>T NCBI36
NG_046960.1:g.11871G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000257527.9:c.180+1942G>A MANE Select ENSP00000257527.5:n.180+1942G>A
ENST00000257527.8:c.180+1942G>A ENSP00000257527.4:n.180+1942G>A
ENST00000517905.1:c.180+1942G>A ENSP00000428654.1:n.180+1942G>A
ENST00000517951.5:c.180+1942G>A ENSP00000428376.1:n.180+1942G>A
NM_033274.4:c.180+1942G>A NP_150377.1:n.180+1942G>A
XM_005266003.2:c.180+1942G>A XP_005266060.1:n.180+1942G>A
NM_033274.5:c.180+1942G>A MANE Select NP_150377.1:n.180+1942G>A
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