Canonical Allele Identifier: CA130184682

Gene: ADAM19

Linked Data

• dbSNP Id: rs552873447
• gnomAD v2: 5-156942265-G-A
• gnomAD v3: 5-157515257-G-A
• gnomAD v4: 5-157515257-G-A
• MyVariant Identifiers: chr5:g.156942265G>A (hg19) ; chr5:g.157515257G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157515257G>A , CM000667.2:g.157515257G>A	GRCh38
NC_000005.9:g.156942265G>A , CM000667.1:g.156942265G>A	GRCh37
NC_000005.8:g.156874843G>A	NCBI36
NG_046960.1:g.65567C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257527.9:c.667-1752C>T MANE Select	ENSP00000257527.5:n.667-1752C>T
ENST00000257527.8:c.667-1752C>T	ENSP00000257527.4:n.667-1752C>T
ENST00000517905.1:c.667-1752C>T	ENSP00000428654.1:n.667-1752C>T
ENST00000517951.5:c.667-1752C>T	ENSP00000428376.1:n.667-1752C>T
NM_033274.4:c.667-1752C>T	NP_150377.1:n.667-1752C>T
XM_005266003.2:c.667-1752C>T	XP_005266060.1:n.667-1752C>T
XM_011534680.1:c.-135-1752C>T	XP_011532982.1:n.-135-1752C>T
XM_011534681.1:c.-145-1752C>T	XP_011532983.1:n.-145-1752C>T
NM_033274.5:c.667-1752C>T MANE Select	NP_150377.1:n.667-1752C>T